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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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210 records meeting your search criteria returned- Product Code: JDR Report Date From: 1/1/2021 Report Date To: 12/31/2021

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ManufacturerBrand NameDate Report Received
DEPUY MITEK LLC US GII QA+ O/C CP-2 *EA 08/05/2021
DEPUY MITEK LLC US GII QA+ O/C CP-2 *EA 08/05/2021
DEPUY MITEK LLC US GII QA+ O/C CP-2 *EA 08/05/2021
DEPUY MITEK LLC US GII QA+ O/C CP-2 *EA 08/05/2021
DEPUY MITEK LLC US GII QA+ O/C CP-2 *EA 08/05/2021
DEPUY MITEK LLC US GII QA+ O/C CP-2 *EA 08/05/2021
SMITH & NEPHEW, INC. MNITAC 2.0 TI W/NDL 22-0 ULTRABRAID 07/29/2021
WRIGHTS LANE SYNTHES USA PRODUCTS LLC SPEEDTITAN(TM) IMPLANT KIT 15 X 15 MM 07/28/2021
SYNTHES GMBH SPEED SHIFT 15X20X20 OFFSET 8MM IMPLANT 07/19/2021
ZIMMER BIOMET, INC. #7 PE ZIPLOOP EXT TOGGLELOC 07/19/2021
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