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	<channel>
		<title>PMA Decisions Rendered since September 01, 2026</title>
		<description>U.S. Food and Drug Administration - Center for Devices and Radiological Health</description>
		<link>https://www.fda.gov/medical-devices/premarket-submissions/premarket-approval-pma</link>
		<language>en-us</language>
		<lastBuildDate>Thu, 08 Oct  2026 05:28:23 GMT</lastBuildDate>
		<webMaster>webmail@oc.fda.gov</webMaster>
		<image>
			<url>https://www.fda.gov/medical-devices</url> 
			<title>U.S. Food and Drug Administration - Center for Devices and Radiological Health</title> 
			<link>https://www.fda.gov/Medical-Devices</link> 
			<description>Premarket approval (PMA) is the FDA process of scientific and regulatory review to evaluate the safety and effectiveness of Class III medical devices. Class III devices are those that support or sustain human life, are of substantial importance in preventing impairment of human health, or which present a potential, unreasonable risk of illness or injury.</description> 
			<width>116</width> 
			<height>70</height>
		</image>



	<item>
		<title>PMA No: N16837/S039</title>
		<description><![CDATA[Device: Artegraft Collagen Vascular Graft - Applicant: LeMaitre Vascular, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=N16837S039</link>
		<pubDate>Fri, 04 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: N970003/S311</title>
		<description><![CDATA[Device: ALTRUA™ 2 (Model S722); ESSENTIO™ (Model L121); PROPONENT™ (Model L221); ACCOLADE™ (Model L321); ALTRUA™ 2 (Models S701, - Applicant: Boston Scientific Corp]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=N970003S311</link>
		<pubDate>Sat, 03 Oct  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: N970012/S212</title>
		<description><![CDATA[Device: AMS 700™ Inflatable Penile Prosthesis (IPP) - Applicant: Boston Scientific Corp]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=N970012S212</link>
		<pubDate>Mon, 14 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P000009/S124</title>
		<description><![CDATA[Device: Ilivia Neo 7 DR-T 429529; Intica Neo 7 DR-T 429558; Intica Neo 5 DR-T 429568 - Applicant: Biotronik, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P000009S124</link>
		<pubDate>Fri, 25 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P000009/S130</title>
		<description><![CDATA[Device: PSW 2601.U, NEO 2601.U, Acticor Sky DR-T, Rivacor Sky DR-T, Rivacor Rise DR-T, Rivacor Aura DR-T - Applicant: Biotronik, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P000009S130</link>
		<pubDate>Thu, 17 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P000009/S133</title>
		<description><![CDATA[Device: Acticor Sky DR-T, Rivacor Sky DR-T, Rivacor Rise DR-T, Rivacor Aura DR-T, Acticor 7 DR-T, Rivacor 7 DR-T, Rivacor 5 DR-T - Applicant: Biotronik, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P000009S133</link>
		<pubDate>Fri, 25 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P000015/S057</title>
		<description><![CDATA[Device: Cochlear Auditory Brainstem Implant System - Applicant: Cochlear Americas]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P000015S057</link>
		<pubDate>Mon, 28 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P000053/S142</title>
		<description><![CDATA[Device: AMS 800™ Artificial Urinary Sphincter (AUS) - Applicant: Boston Scientific Corp]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P000053S142</link>
		<pubDate>Mon, 14 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P010007/S028</title>
		<description><![CDATA[Device: IMMULITE Systems AFP - Applicant: Siemens Healthcare Diagnostics, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P010007S028</link>
		<pubDate>Tue, 22 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P010029/S043</title>
		<description><![CDATA[Device: EUFLEXXA® (1% sodium hyaluronate) - Applicant: Ferring Pharmaceuticals, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P010029S043</link>
		<pubDate>Wed, 02 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P010030/S201</title>
		<description><![CDATA[Device: LifeVest® Wearable Defibrillator - Applicant: Zoll Manufacturing Corporation]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P010030S201</link>
		<pubDate>Wed, 09 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P010030/S203</title>
		<description><![CDATA[Device: LifeVest® Wearable Defibrillator - Applicant: Zoll Manufacturing Corporation]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P010030S203</link>
		<pubDate>Tue, 29 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P010031/S932</title>
		<description><![CDATA[Device: Cobalt MRI CRT-D, Cobalt XT MRI CRT-D, Crome MRI CRT-D - Applicant: Medtronic Cardiac Rhythm Disease Management]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P010031S932</link>
		<pubDate>Fri, 25 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P010032/S251</title>
		<description><![CDATA[Device: Quattrode®; Octrode™; Penta™; Lamitrode™; Tripole™; TriCentrus™ Lead Extensions - Applicant: ABBOTT MEDICAL]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P010032S251</link>
		<pubDate>Fri, 18 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P010032/S260</title>
		<description><![CDATA[Device: Proclaim family of SCS IPG - Applicant: ABBOTT MEDICAL]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P010032S260</link>
		<pubDate>Wed, 23 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P010032/S261</title>
		<description><![CDATA[Device: Spinal Cord Stimulation (SCS) Implantable Pulse Generator (IPG) Charger - Applicant: ABBOTT MEDICAL]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P010032S261</link>
		<pubDate>Fri, 11 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P020018/S070</title>
		<description><![CDATA[Device: Zenith Fenestrated AAA Endovascular Graft, Zenith Iliac Branch - Applicant: Cook, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P020018S070</link>
		<pubDate>Thu, 17 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P020056/S064</title>
		<description><![CDATA[Device: Natrelle Silicone-Filled Breast Implants and Natrelle INSPIRA Silicone-Filled Breast Implants - Applicant: Allergan]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P020056S064</link>
		<pubDate>Tue, 29 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P030005/S257</title>
		<description><![CDATA[Device: VALITUDE™ (Model U125); VALITUDE X4 (Model U128); VISIONIST™ (Models U225, U226); VISIONIST X4 (Model U228) - Applicant: Guidant Corp.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P030005S257</link>
		<pubDate>Sat, 03 Oct  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P030017/S396</title>
		<description><![CDATA[Device: WaveWriter Alpha™ and WaveWriter Alpha™ Prime SCS Systems; Celestia and Celestia Prime SCS Systems - Applicant: Boston Scientific Corp]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P030017S396</link>
		<pubDate>Wed, 09 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P030017/S399</title>
		<description><![CDATA[Device: Precision Spectra SCS Systems; Precision Novi SCS Systems; Precision Montage MRI SCS Systems; Spectra Wave Writer SCS Sy - Applicant: Boston Scientific Corp]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P030017S399</link>
		<pubDate>Tue, 22 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P030031/S142</title>
		<description><![CDATA[Device: THERMOCOOL SMARTTOUCH® SF Catheter - Applicant: Biosense Webster, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P030031S142</link>
		<pubDate>Wed, 02 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P030031/S146</title>
		<description><![CDATA[Device: EZ STEER THERMOCOOL NAV BI-DIRECTIONAL ELECTROPHYSIOLOGY CATHETER; THERMOCOOL SMARTTOUCH BI-DIRECTIONAL NAVIGATION CATHE - Applicant: Biosense Webster, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P030031S146</link>
		<pubDate>Tue, 15 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P030050/S056</title>
		<description><![CDATA[Device: SCULPTRA® (injectable poly-L Lactic acid) - Applicant: Q-Med AB]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P030050S056</link>
		<pubDate>Thu, 17 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P040014/S052</title>
		<description><![CDATA[Device: Therapy™ (including Bi-Directional and 4mm Thermistor) Ablation Catheter - Applicant: Irvine Biomedical, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P040014S052</link>
		<pubDate>Thu, 03 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P040021/S063</title>
		<description><![CDATA[Device: Epic™ Plus, Epic™ Plus Supra, Epic™ Max, Epic™ Elite, Epic™ Supra G3 Tissue Heart Valves - Applicant: ABBOTT MEDICAL]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P040021S063</link>
		<pubDate>Fri, 18 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P040036/S101</title>
		<description><![CDATA[Device: THERMOCOOL SMARTTOUCH BI-DIRECTIONAL NAVIGATION CATHETER; THERMOCOOL SMARTTOUCH UNI-DIRECTIONAL NAVIGATION CATHETER - Applicant: Biosense Webster, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P040036S101</link>
		<pubDate>Tue, 15 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P040042/S060</title>
		<description><![CDATA[Device: Therapy™ Dual-8™ Ablation Catheter - Applicant: Irvine Biomedical,Inc.(Ibi)]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P040042S060</link>
		<pubDate>Thu, 03 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P040045/S145</title>
		<description><![CDATA[Device: VISTAKON (SENOFILCON A) CONTACT LENS, CLEAR AND VISIBILITY TINTED WITH UV BLOCKER - Applicant: Vistakon, Division of Johnson &amp; Johnson Vision Car]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P040045S145</link>
		<pubDate>Wed, 02 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P050023/S204</title>
		<description><![CDATA[Device: Ilivia 7 VR-T DX 404624; Intica 7 VR-T DX 404633; Intica 5 VR-T DX 404688; Ilivia 7 VR-T 404625; Intica 7 VR-T 404634; I - Applicant: Biotronik, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P050023S204</link>
		<pubDate>Fri, 25 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P050023/S211</title>
		<description><![CDATA[Device: PSW 2601.U, NEO 2601.U, Acticor Sky HF-T, Rivacor Sky HF-T, Rivacor Rise HF-T, Rivacor Aura HF-T, Acticor Sky HF-T QP, R - Applicant: Biotronik, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P050023S211</link>
		<pubDate>Thu, 17 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P050023/S214</title>
		<description><![CDATA[Device: Acticor Sky HF-T, Rivacor Sky HF-T, Rivacor Rise HF-T, Rivacor Aura HF-T, Acticor Sky HF-T QP, Rivacor Sky HF-T QP, Riva - Applicant: Biotronik, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P050023S214</link>
		<pubDate>Fri, 25 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P060005/S027</title>
		<description><![CDATA[Device: IMMULITE Systems Free PSA - Applicant: Siemens Medical Solutions Diagnostics Limited]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P060005S027</link>
		<pubDate>Tue, 22 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P060011/S045</title>
		<description><![CDATA[Device: RayOne Galaxy; Model RAO605G, RayOne Galaxy Toric; Model RAO615X - Applicant: Rayner Intraocular Lenses , Ltd.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P060011S045</link>
		<pubDate>Thu, 24 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P060022/S038</title>
		<description><![CDATA[Device: Akreos posterior chamber intraocular lens - Applicant: Bausch &amp; Lomb, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P060022S038</link>
		<pubDate>Thu, 03 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P060037/S099</title>
		<description><![CDATA[Device: NexGen LPS-Flex Mobile and LPS-Mobile Bearing Knee System - Applicant: Zimmer, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P060037S099</link>
		<pubDate>Thu, 24 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P060040/S128</title>
		<description><![CDATA[Device: HeartMate II LVAS - Applicant: ABBOTT MEDICAL]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P060040S128</link>
		<pubDate>Thu, 01 Oct  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P070001/S031</title>
		<description><![CDATA[Device: prodisc® C Nova - Applicant: Centinel Spine, LLC]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P070001S031</link>
		<pubDate>Wed, 09 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P070008/S172</title>
		<description><![CDATA[Device: Edora 8 HF-T QP 407137 Edora 8 HF-T 407138 Evity 8 HF-T QP 407139 Evity 8 HF-T 407140 Enitra 8 HF-T QP 407141 Enitra 8 H - Applicant: Biotronik, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P070008S172</link>
		<pubDate>Fri, 25 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P070008/S179</title>
		<description><![CDATA[Device: PSW 2601.U, NEO 2601.U - Applicant: Biotronik, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P070008S179</link>
		<pubDate>Thu, 17 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P070026/S129</title>
		<description><![CDATA[Device: CERAMAX CERAMIC HIP SYSTEM - Applicant: DePuy Orthopaedics, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P070026S129</link>
		<pubDate>Fri, 04 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P080011/S204</title>
		<description><![CDATA[Device: BIOFINITY (COMFILCON A) - Applicant: CooperVision, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P080011S204</link>
		<pubDate>Wed, 02 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P080020/S056</title>
		<description><![CDATA[Device: Gel-One - Applicant: Seikagaku Corp.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P080020S056</link>
		<pubDate>Fri, 04 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P080025/S352</title>
		<description><![CDATA[Device: InterStim™ Therapy System, Verify™ Evaluation System - Applicant: Medtronic Neuromodulation]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P080025S352</link>
		<pubDate>Mon, 14 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P100010/S154</title>
		<description><![CDATA[Device: STOP Persistent AF - Applicant: Medtronic Cryocath, LP]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P100010S154</link>
		<pubDate>Fri, 25 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P100034/S045</title>
		<description><![CDATA[Device: Novocure GmbH’s Optune Gio - Applicant: Novocure, GmbH]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P100034S045</link>
		<pubDate>Fri, 18 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P100034/S046</title>
		<description><![CDATA[Device: Optune HFE Transducer Arrays - Applicant: Novocure, GmbH]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P100034S046</link>
		<pubDate>Wed, 16 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P100044/S060</title>
		<description><![CDATA[Device: Propel Family Products - Applicant: Intersect Ent.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P100044S060</link>
		<pubDate>Wed, 23 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P100044/S061</title>
		<description><![CDATA[Device: PROPEL - Applicant: Intersect Ent.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P100044S061</link>
		<pubDate>Tue, 22 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P100045/S091</title>
		<description><![CDATA[Device: CardioMEMS HF System; Merlin.net PCN HF Portal (Model MN6000); CardioMEMS Backend Web Application (Model CM4000); HF Clo - Applicant: ABBOTT MEDICAL]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P100045S091</link>
		<pubDate>Wed, 30 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P100045/S092</title>
		<description><![CDATA[Device: CardioMEMS PA Sensor and Delivery System (CM2000); CardioMEMS™ HF System - Applicant: ABBOTT MEDICAL]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P100045S092</link>
		<pubDate>Fri, 11 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P100045/S093</title>
		<description><![CDATA[Device: CardioMEMS PA Sensor and Delivery System - Applicant: ABBOTT MEDICAL]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P100045S093</link>
		<pubDate>Wed, 30 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P100046/S021</title>
		<description><![CDATA[Device: Synergy Ablation System - Applicant: AtriCure, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P100046S021</link>
		<pubDate>Thu, 24 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P100047/S241</title>
		<description><![CDATA[Device: HeartWare® HVAD System - Applicant: Medtronic]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P100047S241</link>
		<pubDate>Wed, 23 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P110002/S040</title>
		<description><![CDATA[Device: Mobi-C® Cervical Disc Prosthesis for use at One Level - Applicant: Highridge Medical, LLC]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P110002S040</link>
		<pubDate>Wed, 16 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P110009/S040</title>
		<description><![CDATA[Device: Mobi-C® Cervical Disc Prosthesis for use at Two Levels - Applicant: Highridge Medical, LLC]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P110009S040</link>
		<pubDate>Wed, 16 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P110019/S145</title>
		<description><![CDATA[Device: XIENCE PRO5 Everolimus Eluting Coronary Stent System (XIENCE PRO5), XIENCE Skypoint Everolimus Eluting Coronary Stent Sy - Applicant: Abbott Vascular]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P110019S145</link>
		<pubDate>Thu, 01 Oct  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P110042/S216</title>
		<description><![CDATA[Device: EMBLEM™ Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) high voltage (HV) Capacitor - Applicant: Boston Scientific Corporation]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P110042S216</link>
		<pubDate>Fri, 02 Oct  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P120016/S043</title>
		<description><![CDATA[Device: VASCADE 5F Vascular Closure System - Applicant: Cardiva Medical, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P120016S043</link>
		<pubDate>Thu, 10 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P130016/S061</title>
		<description><![CDATA[Device: Cochlear Hybrid Implant System - Applicant: Cochlear Americas]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P130016S061</link>
		<pubDate>Mon, 28 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P140009/S139</title>
		<description><![CDATA[Device: Infinity DBS IPG - Applicant: ABBOTT MEDICAL]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P140009S139</link>
		<pubDate>Wed, 23 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P140009/S140</title>
		<description><![CDATA[Device: Deep Brain Stimulation (DBS) Implantable Pulse Generator (IPG) Charger - Applicant: ABBOTT MEDICAL]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P140009S140</link>
		<pubDate>Fri, 11 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P140010/S106</title>
		<description><![CDATA[Device: IN.PACT 018 Paclitaxel-Coated Percutaneous Transluminal Angioplasty (PTA) Balloon Catheter - Applicant: Medtronic, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P140010S106</link>
		<pubDate>Thu, 24 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P140019/S014</title>
		<description><![CDATA[Device: i-F ACTOR® Peptide Enhanced Graft Substitute - Applicant: Cerapedics, LLC]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P140019S014</link>
		<pubDate>Wed, 16 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P140029/S058</title>
		<description><![CDATA[Device: Restylane® Contour - Applicant: Q-Med AB]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P140029S058</link>
		<pubDate>Fri, 18 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P140030/S025</title>
		<description><![CDATA[Device: Astron Peripheral Self-Expanding Nitinol Stent System - Applicant: Biotronik AG]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P140030S025</link>
		<pubDate>Fri, 11 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P140031/S209</title>
		<description><![CDATA[Device: Edwards Crimper (9600LDS23, 9600LDS26, 9600LDS29, 9750CM20, 9750CM23, 9750CM26, 9750CM29) - Applicant: Edwards Lifesciences, LLC]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P140031S209</link>
		<pubDate>Wed, 23 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P150004/S100</title>
		<description><![CDATA[Device: Proclaim DRG IPG - Applicant: ABBOTT MEDICAL]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P150004S100</link>
		<pubDate>Wed, 23 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P150012/S191</title>
		<description><![CDATA[Device: ESSENTIO MRI (Model L131); PROPONENT MRI (Model L231); ACCOLADE MRI (Model L331); ESSENTIO™ MRI (Models L110, L111); PRO - Applicant: Boston Scientific]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P150012S191</link>
		<pubDate>Sat, 03 Oct  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P150013/S034</title>
		<description><![CDATA[Device: PD-L1 IHC 22C3 pharmDx - Applicant: Agilent Technologies, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P150013S034</link>
		<pubDate>Mon, 21 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P150013/S035</title>
		<description><![CDATA[Device: PD-L1 IHC 22C3 pharmDx - Applicant: Agilent Technologies, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P150013S035</link>
		<pubDate>Fri, 11 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P150025/S019</title>
		<description><![CDATA[Device: PD-L1 IHC 28-8 pharmDx - Applicant: Agilent Technologies, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P150025S019</link>
		<pubDate>Mon, 21 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P150025/S020</title>
		<description><![CDATA[Device: PD-L1 IHC 28-8 pharmDx - Applicant: Agilent Technologies, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P150025S020</link>
		<pubDate>Fri, 11 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P150031/S084</title>
		<description><![CDATA[Device: VERCISE DEEP BRAIN STIMULATION (DBS) SYSTEM - Applicant: Boston Scientific Corp]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P150031S084</link>
		<pubDate>Sun, 13 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P150031/S098</title>
		<description><![CDATA[Device: Vercise Genus DBS Systems; Vercise Gevia DBS Systems - Applicant: Boston Scientific Corp]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P150031S098</link>
		<pubDate>Tue, 22 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P150033/S230</title>
		<description><![CDATA[Device: Micra Functional Testing on pNGHT and NGHT - Applicant: Medtronic, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P150033S230</link>
		<pubDate>Tue, 08 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P150038/S044</title>
		<description><![CDATA[Device: Exablate Model 4000 System - Applicant: Insightec]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P150038S044</link>
		<pubDate>Wed, 16 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P160017/S140</title>
		<description><![CDATA[Device: MiniMed 780G System - Applicant: Medtronic Minimed, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P160017S140</link>
		<pubDate>Tue, 29 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P160022/S054</title>
		<description><![CDATA[Device: X Series®, R Series®, AED Pro®, AED 3™ BLS Professional Defibrillators, Pro-Padz Radiotransparent Electrode, SurePower™ - Applicant: ZOLL Medical Corporation]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P160022S054</link>
		<pubDate>Fri, 02 Oct  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P160025/S026</title>
		<description><![CDATA[Device: Pulsar-18 T3 Peripheral Self-Expanding Nitinol Stent System - Applicant: Biotronik AG]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P160025S026</link>
		<pubDate>Fri, 11 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P160026/S069</title>
		<description><![CDATA[Device: LIFEPAK® 35 monitor/defibrillator - Applicant: Physio-Control, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P160026S069</link>
		<pubDate>Wed, 02 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P160026/S073</title>
		<description><![CDATA[Device: LIFEPAK® 15 monitor/defibrillator - Applicant: Physio-Control, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P160026S073</link>
		<pubDate>Thu, 10 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P160026/S074</title>
		<description><![CDATA[Device: LIFEPAK 1000 DEFIBRILLATOR, LIFEPAK 20 DEFIBRILLATOR/ MONITOR, LIFEPAK 20E DEFIBRILLATOR/ MONITOR, LIFEPAK 15 MONITOR/DE - Applicant: Physio-Control, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P160026S074</link>
		<pubDate>Thu, 24 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P160035/S057</title>
		<description><![CDATA[Device: EXCOR Pediatric Ventricular Assist Device - Applicant: Berlin Heart, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P160035S057</link>
		<pubDate>Thu, 01 Oct  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P160054/S134</title>
		<description><![CDATA[Device: HeartMate 3™ Left Ventricular Assist System - Applicant: ABBOTT MEDICAL]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P160054S134</link>
		<pubDate>Wed, 09 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P160054/S135</title>
		<description><![CDATA[Device: HeartMate 3 LVAS - Applicant: ABBOTT MEDICAL]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P160054S135</link>
		<pubDate>Thu, 01 Oct  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P160055/S056</title>
		<description><![CDATA[Device: RxSight Light Adjustable Lens and Light Delivery Device - Applicant: Rxsight, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P160055S056</link>
		<pubDate>Thu, 03 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P170012/S032</title>
		<description><![CDATA[Device: HEMOBLAST™ Bellows - Applicant: Dilon Technologies, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P170012S032</link>
		<pubDate>Thu, 03 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P170013/S013</title>
		<description><![CDATA[Device: Intraluminal Support Device LVIS/LVIS Jr./LVIS EVO - Applicant: MicroVention, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P170013S013</link>
		<pubDate>Wed, 16 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P170019/S069</title>
		<description><![CDATA[Device: FoundationOne CDx - Applicant: Foundation Medicine, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P170019S069</link>
		<pubDate>Wed, 16 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P170030/S066</title>
		<description><![CDATA[Device: ORSIRO Sirolimus Eluting Coronary Stent System - Applicant: Biotronik AG]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P170030S066</link>
		<pubDate>Thu, 24 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P170035/S021</title>
		<description><![CDATA[Device: Bausch + Lomb Ultra (samfilcon A) Contact Lenses - Applicant: Bausch and Lomb, Inc.,]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P170035S021</link>
		<pubDate>Mon, 14 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P170038/S032</title>
		<description><![CDATA[Device: CentriMag™ Circulatory Support System - Applicant: Abbott]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P170038S032</link>
		<pubDate>Wed, 02 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P170038/S033</title>
		<description><![CDATA[Device: CentriMag™ Circulatory Support System - Applicant: Abbott]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P170038S033</link>
		<pubDate>Fri, 02 Oct  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P170043/S023</title>
		<description><![CDATA[Device: Glaukos® iStent inject® W Trabecular Micro-Bypass System, Glaukos® iStent inject® W Trabecular Micro-Bypass System with - Applicant: Glaukos Corporation]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P170043S023</link>
		<pubDate>Thu, 01 Oct  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P180002/S032</title>
		<description><![CDATA[Device: Zephyr Endobronchial Valve System - Applicant: Pulmonx Corporation]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P180002S032</link>
		<pubDate>Fri, 11 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P180014/S014</title>
		<description><![CDATA[Device: XPS™ with Steen Solution™ Perfusate - Applicant: Xvivo Perfusion, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P180014S014</link>
		<pubDate>Wed, 16 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P180032/S024</title>
		<description><![CDATA[Device: Cerene® Cryotherapy Device - Applicant: Channel Medsystems, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P180032S024</link>
		<pubDate>Tue, 15 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P180036/S044</title>
		<description><![CDATA[Device: OPTIMIZER Smart System - Applicant: Impulse Dynamics (Usa), Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P180036S044</link>
		<pubDate>Thu, 24 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P180047/S046</title>
		<description><![CDATA[Device: LIAISON® QuantiFERON®-TB Gold Plus II. - Applicant: DiaSorin, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P180047S046</link>
		<pubDate>Thu, 24 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P190032/S032</title>
		<description><![CDATA[Device: FoundationOne Liquid CDx (F1LCDx) - Applicant: Foundation Medicine, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P190032S032</link>
		<pubDate>Fri, 18 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P200002/S015</title>
		<description><![CDATA[Device: EPi- Sense ST Coagulation System - Applicant: AtriCure, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P200002S015</link>
		<pubDate>Thu, 24 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P200010/S024</title>
		<description><![CDATA[Device: Guardant360® CDx - Applicant: Guardant Health, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P200010S024</link>
		<pubDate>Fri, 04 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P200010/S029</title>
		<description><![CDATA[Device: Guardant360 CDx - Applicant: Guardant Health, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P200010S029</link>
		<pubDate>Fri, 18 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P200015/S083</title>
		<description><![CDATA[Device: Edwards Crimper (9600LDS20, 9600LDS23, 9600LDS26, 9600LDS29) - Applicant: Edwards Lifesciences, LLC]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P200015S083</link>
		<pubDate>Wed, 23 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P200036/S012</title>
		<description><![CDATA[Device: eCoin Peripheral Neurostimulator - Applicant: Boston Scientific Corporation]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P200036S012</link>
		<pubDate>Wed, 09 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P200037/S021</title>
		<description><![CDATA[Device: ASSURE Wearable Cardioverter Defibrillator (WCD) System - Applicant: Kestra Medical Technologies, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P200037S021</link>
		<pubDate>Mon, 28 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P200039/S025</title>
		<description><![CDATA[Device: SHOCKWAVE™ INTRAVASCULAR LITHOTRIPSY (IVL) SYSTEM WITH SHOCKWAVE C2/C2+ CORONARY IVL CATHETER - Applicant: Shockwave Medical, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P200039S025</link>
		<pubDate>Fri, 11 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P200046/S052</title>
		<description><![CDATA[Device: Harmony TPV System - Applicant: Medtronic, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P200046S052</link>
		<pubDate>Wed, 30 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P210006/S018</title>
		<description><![CDATA[Device: Thoraflex™ Hybrid - Applicant: Vascutek, Ltd.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P210006S018</link>
		<pubDate>Tue, 08 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P210007/S015</title>
		<description><![CDATA[Device: Vivistim® System - Applicant: Mobia Medical, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P210007S015</link>
		<pubDate>Wed, 16 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P210011/S002</title>
		<description><![CDATA[Device: xT CDx - Applicant: Tempus AI, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P210011S002</link>
		<pubDate>Wed, 02 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P210026/S003</title>
		<description><![CDATA[Device: Ki-67 IHC MIB-1 pharmDx (Dako Omnis) - Applicant: Agilent Technologies, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P210026S003</link>
		<pubDate>Fri, 11 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P210027/S018</title>
		<description><![CDATA[Device: QDOT MICRO™ System - Applicant: Biosense Webster, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P210027S018</link>
		<pubDate>Thu, 10 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P210027/S019</title>
		<description><![CDATA[Device: QDOT MICRO BI-DIRECTIONAL NAVIGATION CATHETER; QDOT MICRO UNI-DIRECTIONAL NAVIGATION CATHETER - Applicant: Biosense Webster, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P210027S019</link>
		<pubDate>Tue, 15 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P220002/S011</title>
		<description><![CDATA[Device: TOPS™ System - Applicant: Premia Spine, Ltd.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P220002S011</link>
		<pubDate>Wed, 09 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P220003/S028</title>
		<description><![CDATA[Device: PASCAL Ace with Capture Clarity™ Valve Repair System – MR Implant System - Applicant: Edwards Lifesciences, LLC]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P220003S028</link>
		<pubDate>Wed, 23 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P220003/S033</title>
		<description><![CDATA[Device: PASCAL Precision Transcatheter Valve Repair System - Applicant: Edwards Lifesciences, LLC]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P220003S033</link>
		<pubDate>Wed, 09 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P220013/S028</title>
		<description><![CDATA[Device: TactiFlex™ Duo Ablation Catheter, Sensor Enabled™ (A-TFDM-D, A-TFDM-F, A-TFDM-J, A-TFDM-DD, A-TFDM-DF, A-TFDM-FF, A-TFDM - Applicant: ABBOTT MEDICAL]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P220013S028</link>
		<pubDate>Fri, 04 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P220013/S034</title>
		<description><![CDATA[Device: TactiFlex™ Ablation Catheter, Sensor Enabled™ - Applicant: ABBOTT MEDICAL]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P220013S034</link>
		<pubDate>Tue, 22 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P220014/S013</title>
		<description><![CDATA[Device: CraniSeal™ Dural Sealant - Applicant: Pramand, LLC]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P220014S013</link>
		<pubDate>Thu, 01 Oct  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P220026/S014</title>
		<description><![CDATA[Device: Symplicity Spyral™ Renal Denervation System - Applicant: Medtronic, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P220026S014</link>
		<pubDate>Thu, 10 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P220030/S012</title>
		<description><![CDATA[Device: UNIPURE C3F8 Ophthalmic Gas in the UNIFEYE Gas Delivery System - Applicant: Alcon Research, LLC]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P220030S012</link>
		<pubDate>Wed, 30 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P230001/S014</title>
		<description><![CDATA[Device: ColoSense® - Applicant: Geneoscopy, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P230001S014</link>
		<pubDate>Tue, 08 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P230003/S019</title>
		<description><![CDATA[Device: Alinity m HR HPV - Applicant: Abbott Molecular, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P230003S019</link>
		<pubDate>Wed, 02 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P230005/S002</title>
		<description><![CDATA[Device: Motiva SmoothSilk Round Ergonomix Silicone Gel-Filled Breast Implants, Motiva SmoothSilk Round Silicone Gel-Filled Breas - Applicant: Motiva USA, LLC]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P230005S002</link>
		<pubDate>Fri, 02 Oct  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P230005/S005</title>
		<description><![CDATA[Device: Motiva SmoothSilk® Round and Round Ergonomix® Silicone Gel-Filled Breast Implants - Applicant: Motiva USA, LLC]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P230005S005</link>
		<pubDate>Fri, 25 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P230009/S020</title>
		<description><![CDATA[Device: Shield - Applicant: Guardant Health, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P230009S020</link>
		<pubDate>Wed, 16 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P230011/S008</title>
		<description><![CDATA[Device: TruSight Oncology Comprehensive - Applicant: Illumina, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P230011S008</link>
		<pubDate>Fri, 04 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P230012/S012</title>
		<description><![CDATA[Device: UNIPURE SF6 Ophthalmic Gas in the UNIFEYE Gas Delivery System - Applicant: Alcon Research, LLC]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P230012S012</link>
		<pubDate>Wed, 30 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P230013/S027</title>
		<description><![CDATA[Device: EVOQUE Tricuspid Valve Replacement System - Applicant: Edwards Lifesciences, LLC]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P230013S027</link>
		<pubDate>Wed, 16 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P230016/S003</title>
		<description><![CDATA[Device: MAGE-A4 IHC 1F9 pharmDx - Applicant: Agilent Technologies, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P230016S003</link>
		<pubDate>Tue, 15 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P230016/S004</title>
		<description><![CDATA[Device: MAGE-A4 IHC 1F9 pharmDx - Applicant: Agilent Technologies, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P230016S004</link>
		<pubDate>Mon, 21 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P230016/S005</title>
		<description><![CDATA[Device: MAGE-A4 IHC 1F9 pharmDx - Applicant: Agilent Technologies, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P230016S005</link>
		<pubDate>Fri, 11 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P230019/S005</title>
		<description><![CDATA[Device: MediBeacon Transdermal GFR System - Applicant: Medibeacon, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P230019S005</link>
		<pubDate>Fri, 02 Oct  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P230030/S024</title>
		<description><![CDATA[Device: FARASTAR™ Pulsed Field Ablation (PFA) Generator; FARASTAR™ Mapping System Module (MSM); FARASTAR™ Recording System Modul - Applicant: Farapulse, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P230030S024</link>
		<pubDate>Fri, 04 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P230030/S025</title>
		<description><![CDATA[Device: FARAPULSE™ Pulsed Field Ablation System (FARAWAVE™ Pulsed Field Ablation Catheter, FARASTAR™ Catheter Connection Cable, - Applicant: Farapulse, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P230030S025</link>
		<pubDate>Fri, 02 Oct  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P230036/S020</title>
		<description><![CDATA[Device: Esprit™ BTK Everolimus Eluting Resorbable Scaffold System - Applicant: ABBOTT MEDICAL]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P230036S020</link>
		<pubDate>Thu, 24 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P230040/S033</title>
		<description><![CDATA[Device: Cordella Pulmonary Artery Sensor System (CorPASS) - Applicant: Endotronix, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P230040S033</link>
		<pubDate>Fri, 25 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P240001/S003</title>
		<description><![CDATA[Device: PearlMatrixTM Peptide Enhanced Bone Graft - Applicant: Cerapedics, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P240001S003</link>
		<pubDate>Wed, 16 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P240005/S007</title>
		<description><![CDATA[Device: enVista Envy™ hydrophobic acrylic intraocular lens (IOL) - Applicant: Bausch &amp; Lomb, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P240005S007</link>
		<pubDate>Thu, 03 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P240005/S008</title>
		<description><![CDATA[Device: enVista Envy™ Hydrophobic Acrylic Intraocular Lens - Applicant: Bausch &amp; Lomb, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P240005S008</link>
		<pubDate>Wed, 30 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P240006/S019</title>
		<description><![CDATA[Device: VARIPULSE™ Platform (VARIPULSE™ Catheter; TRUPULSE™ Generator; Sterile Interface Cable; nGEN™ Pump) - Applicant: Biosense Webster, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P240006S019</link>
		<pubDate>Thu, 10 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P240006/S020</title>
		<description><![CDATA[Device: VARIPULSE BI-DIRECTIONAL CATHETER - Applicant: Biosense Webster, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P240006S020</link>
		<pubDate>Tue, 15 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P240011/S016</title>
		<description><![CDATA[Device: Altaviva™ - Applicant: Medtronic Neuromodulation]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P240011S016</link>
		<pubDate>Mon, 14 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P240012/S008</title>
		<description><![CDATA[Device: AeroPace® System - Applicant: Lungpacer Medical USA, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P240012S008</link>
		<pubDate>Fri, 25 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P240013/S031</title>
		<description><![CDATA[Device: Sphere-9 Catheter and Affera Ablation System - Applicant: Medtronic, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P240013S031</link>
		<pubDate>Fri, 02 Oct  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P240027/S007</title>
		<description><![CDATA[Device: SpineSeal™ Spine Sealant - Applicant: Pramand, LLC]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P240027S007</link>
		<pubDate>Fri, 11 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P240038/S003</title>
		<description><![CDATA[Device: FINEVISION HP Trifocal IOLs - Applicant: Beaver Visitec International, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P240038S003</link>
		<pubDate>Fri, 25 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P240040/S005</title>
		<description><![CDATA[Device: Oncomine™ Dx Express Test - Applicant: Life Technologies Corporation]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P240040S005</link>
		<pubDate>Wed, 09 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P250003/S009</title>
		<description><![CDATA[Device: Embrace Hydrogel Embolic System - Applicant: Instylla, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P250003S009</link>
		<pubDate>Thu, 03 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P250004/S001</title>
		<description><![CDATA[Device: MMR IHC Panel pharmDx (Dako Omnis) - Applicant: Agilent Technologies, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P250004S001</link>
		<pubDate>Fri, 11 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P250009/S002</title>
		<description><![CDATA[Device: SQUID Liquid Embolic Agent (LEA) - Applicant: Balt USA, LLC]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P250009S002</link>
		<pubDate>Wed, 09 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P250011/S006</title>
		<description><![CDATA[Device: ProVee System for BPH - Applicant: Proverum, Ltd.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P250011S006</link>
		<pubDate>Thu, 24 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P250020/S005</title>
		<description><![CDATA[Device: Belotero Volume (+) Lidocaine Dermal Filler - Applicant: Merz North America, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P250020S005</link>
		<pubDate>Thu, 10 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P250023/S001</title>
		<description><![CDATA[Device: Allurion™ Gastric Balloon System - Applicant: Allurion Technologies, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P250023S001</link>
		<pubDate>Wed, 09 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P250023/S002</title>
		<description><![CDATA[Device: Allurion™ Gastric Balloon System - Applicant: Allurion Technologies, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P250023S002</link>
		<pubDate>Wed, 23 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P250028/S003</title>
		<description><![CDATA[Device: Synergy Disc - Applicant: Synergy Spine Solutions, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P250028S003</link>
		<pubDate>Thu, 17 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P250033/S004</title>
		<description><![CDATA[Device: NEXUS Aortic Arch Stent Graft System - Applicant: Endospan , Ltd.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P250033S004</link>
		<pubDate>Mon, 21 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P250041</title>
		<description><![CDATA[Device: SELUTION SLR™ 014 PTCA Drug-Eluting Balloon - Applicant: MedAlliance, LLC]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P250041</link>
		<pubDate>Fri, 18 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P250042/S002</title>
		<description><![CDATA[Device: BAGUERA®C Cervical Disc Prosthesis - Applicant: Spineart USA, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P250042S002</link>
		<pubDate>Tue, 22 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P250046</title>
		<description><![CDATA[Device: OncoMate® MSI Dx Analysis System - Applicant: Promega Corporation]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P250046</link>
		<pubDate>Tue, 15 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P250050</title>
		<description><![CDATA[Device: Liverty™ TIPS Stent Graft - Applicant: Bard Peripheral Vascular, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P250050</link>
		<pubDate>Fri, 25 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P250051</title>
		<description><![CDATA[Device: Juveena Hydrogel System - Applicant: Rejoni, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P250051</link>
		<pubDate>Mon, 28 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P260007</title>
		<description><![CDATA[Device: Autus Size-Adjustable Valve - Applicant: Edwards Lifesciences, LLC]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P260007</link>
		<pubDate>Thu, 01 Oct  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P800002/S036</title>
		<description><![CDATA[Device: Avitene Microfibrillar Collagen Hemostat (MCH) Non-Woven Web Webber - Applicant: C.R. Bard, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P800002S036</link>
		<pubDate>Tue, 29 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P810006/S115</title>
		<description><![CDATA[Device: Collastat™ Absorbable Collagen Hemostatic Sponge and Collastat™ Absorbable Collagen Hemostatic Agent - Microfibrillar Fo - Applicant: Integra LifeSciences Corporation]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P810006S115</link>
		<pubDate>Fri, 18 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P830055/S351</title>
		<description><![CDATA[Device: Attune Revision Knee System - Applicant: Depuy, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P830055S351</link>
		<pubDate>Mon, 21 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P830055/S372</title>
		<description><![CDATA[Device: ATTUNE Rotating Platform (RP) Total Knee System, ATTUNE Cementless Rotating Platform (RP) Knee System, ATTUNE Revision R - Applicant: Depuy, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P830055S372</link>
		<pubDate>Wed, 09 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P830055/S374</title>
		<description><![CDATA[Device: LCS(R) TOTAL KNEE SYSTEM, specifically ATTUNE™ Cruciate Retaining (CR), Posterior Stabilized (PS) and Revision Femoral C - Applicant: Depuy, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P830055S374</link>
		<pubDate>Thu, 03 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P830055/S375</title>
		<description><![CDATA[Device: LCS® Total Knee System - Applicant: Depuy, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P830055S375</link>
		<pubDate>Fri, 25 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P830055/S376</title>
		<description><![CDATA[Device: Attune Rotating Platform (RP) Total Knee System and the DePuy P.F.C.™ Sigma™ Rotating Platform (RP) Total Knee System an - Applicant: Depuy, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P830055S376</link>
		<pubDate>Thu, 10 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P840001/S634</title>
		<description><![CDATA[Device: Vanta™with AdaptiveStim™ Technology - Model 977006 - Applicant: Medtronic Neuromodulation]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P840001S634</link>
		<pubDate>Thu, 24 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P840024/S099</title>
		<description><![CDATA[Device: Nucleus® 22 Cochlear Implant System - Applicant: Cochlear Americas]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P840024S099</link>
		<pubDate>Mon, 28 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P840062/S099</title>
		<description><![CDATA[Device: CollaCote™, CollaTape®, CollaPlug®, Absorbable Collagen Wound Dressings for Dental Surgery - Applicant: Integra Lifesciences Corp.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P840062S099</link>
		<pubDate>Fri, 18 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P840064/S094</title>
		<description><![CDATA[Device: VISCOAT™ Ophthalmic Viscosurgical Device; DUOVISC™ Ophthalmic Viscosurgical System; DISCOVISC™ Ophthalmic Viscosurgical - Applicant: Alcon Laboratories]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P840064S094</link>
		<pubDate>Thu, 01 Oct  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P850010/S119</title>
		<description><![CDATA[Device: Helistat® Absorbable Collagen Hemostatic Agent and Helitene® Absorbable Collagen Hemostatic Agent- Fibrillar Form - Applicant: Integra LifeSciences Corporation]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P850010S119</link>
		<pubDate>Fri, 18 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P850064/S056</title>
		<description><![CDATA[Device: LifePulse® High Frequency Ventilator - Applicant: Bunnell, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P850064S056</link>
		<pubDate>Mon, 28 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P890027/S067</title>
		<description><![CDATA[Device: Nucleus® 22 Cochlear Implant System - Applicant: Cochlear Americas]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P890027S067</link>
		<pubDate>Mon, 28 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P890047/S072</title>
		<description><![CDATA[Device: PROVISC™ Ophthalmic Viscosurgical Device - Applicant: Alcon Research, Ltd.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P890047S072</link>
		<pubDate>Thu, 01 Oct  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P900033/S117</title>
		<description><![CDATA[Device: INTEGRA ® Dermal Regeneration Template, Integra® Meshed Dermal Regeneration Template, and Integra® Omnigraft Dermal Rege - Applicant: Integra Lifesciences Corp.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P900033S117</link>
		<pubDate>Fri, 18 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P910056/S063</title>
		<description><![CDATA[Device: enVista hydrophobic acrylic intraocular lens - Applicant: Bausch &amp; Lomb, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P910056S063</link>
		<pubDate>Thu, 03 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P910056/S064</title>
		<description><![CDATA[Device: enVista® Hydrophobic Acrylic Intraocular Lens - Applicant: Bausch &amp; Lomb, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P910056S064</link>
		<pubDate>Wed, 30 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P910056/S065</title>
		<description><![CDATA[Device: enVista Aspire™ Hydrophobic Acrylic Intraocular Lens (IOL) - Applicant: Bausch &amp; Lomb, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P910056S065</link>
		<pubDate>Tue, 29 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P910073/S193</title>
		<description><![CDATA[Device: ENDOTAK LEAD SYSTEM - Applicant: Boston Scientific]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P910073S193</link>
		<pubDate>Thu, 17 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P930027/S041</title>
		<description><![CDATA[Device: IMMULITE Systems PSA - Applicant: Siemens Healthcare Diagnostics, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P930027S041</link>
		<pubDate>Tue, 22 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P950037/S279</title>
		<description><![CDATA[Device: Edora 8 DR-T 407145, Evity 8 DR-T 407146, Enitra 8 DR-T 407147, Enticos 8 DR-T 407148, Evity 6 DR-T 407149, Enitra 6 DR- - Applicant: Biotronik, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P950037S279</link>
		<pubDate>Fri, 25 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P950037/S291</title>
		<description><![CDATA[Device: PSW 2601.U, NEO 2601.U, Amvia Sky HF-T QP, Amvia Sky HF-T, Amvia Edge HF-T QP, Amvia Sky DR-T, Amvia Sky SR-T, Amvia Edg - Applicant: Biotronik, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P950037S291</link>
		<pubDate>Thu, 17 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P960009/S546</title>
		<description><![CDATA[Device: MEDTRONIC ACTIVA TREMOR CONTROL SYSTEM - Applicant: Medtronic, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P960009S546</link>
		<pubDate>Thu, 24 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P960043/S137</title>
		<description><![CDATA[Device: Perclose ProGlide Suture-Mediated Closure System; Perclose ProStyle Suture-Mediated Closure and Repair System - Applicant: Abbott Vascular, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P960043S137</link>
		<pubDate>Thu, 24 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P960058/S177</title>
		<description><![CDATA[Device: HiResolution Bionic Ear System - Applicant: Advanced Bionics]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P960058S177</link>
		<pubDate>Fri, 04 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P960058/S178</title>
		<description><![CDATA[Device: CLARION MULTI-STRATEGY COCHLEAR IMPLANT - Applicant: Advanced Bionics]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P960058S178</link>
		<pubDate>Fri, 18 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P970003/S254</title>
		<description><![CDATA[Device: VNS Therapy® System - Applicant: LivaNova USA, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P970003S254</link>
		<pubDate>Fri, 02 Oct  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P970004/S458</title>
		<description><![CDATA[Device: InterStim™ Therapy System Verify™ Evaluation System - Applicant: Medtronic Neuromodulation]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P970004S458</link>
		<pubDate>Mon, 14 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P970051/S244</title>
		<description><![CDATA[Device: Nucleus® 24 Cochlear Implant System - Applicant: Cochlear Americas]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P970051S244</link>
		<pubDate>Mon, 28 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P980016/S965</title>
		<description><![CDATA[Device: Cobalt MRI ICD, Cobalt XT MRI ICD, Crome MRI ICD - Applicant: Medtronic Cardiac Rhythm Disease Management]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P980016S965</link>
		<pubDate>Fri, 25 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P980018/S027</title>
		<description><![CDATA[Device: HercepTest™ - Applicant: Agilent Technologies Singapore (International) Pte , Ltd.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P980018S027</link>
		<pubDate>Mon, 21 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P980023/S140</title>
		<description><![CDATA[Device: Ilivia Neo 7 VR-T DX 429530; Intica Neo 7 VR-T DX 429559; Intica Neo 5 VR-T DX 429569 - Applicant: Biotronik, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P980023S140</link>
		<pubDate>Fri, 25 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P980023/S146</title>
		<description><![CDATA[Device: Acticor Sky VR-T, Rivacor Sky VR-T, Rivacor Rise VR-T, Rivacor Aura VR-T, Acticor Sky VR-T DX, Rivacor Sky VR-T DX, Riva - Applicant: Biotronik, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P980023S146</link>
		<pubDate>Thu, 17 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P980023/S150</title>
		<description><![CDATA[Device: Pamira S 60; Pamira S 65; Pamira S 75; Pamira SD 60/16; Pamira SD 65/16; Pamira SD 65/18; Pamira SD 75/18; Pamira S DX 6 - Applicant: Biotronik, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P980023S150</link>
		<pubDate>Thu, 10 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P980023/S151</title>
		<description><![CDATA[Device: Acticor Sky VR-T, Rivacor Sky VR-T, Rivacor Rise VR-T, Rivacor Aura VR-T, Acticor Sky VR-T DX, Rivacor Sky VR-T DX, Riva - Applicant: Biotronik, Inc.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P980023S151</link>
		<pubDate>Fri, 25 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P980044/S067</title>
		<description><![CDATA[Device: SUPARTZ FX - Applicant: Seikagaku Corp.]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P980044S067</link>
		<pubDate>Fri, 04 Sep  2026 04:00:00 GMT</pubDate>
	</item>

	<item>
		<title>PMA No: P990004/S080</title>
		<description><![CDATA[Device: SURGIFOAM® Absorbable Gelatin Sponge - Applicant: Ferrosan Meidcal Devices A/S]]></description>
		<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?ID=P990004S080</link>
		<pubDate>Fri, 18 Sep  2026 04:00:00 GMT</pubDate>
	</item>

</channel>