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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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405 records meeting your search criteria returned- Product Code: MQP Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
SYNTHES GMBH UNK - CAGE/SPACERS: CERVIOS 04/23/2021
SYNTHES GMBH UNK - CAGE/SPACERS: CERVIOS 04/23/2021
K2M, INC. UNKNOWN_K2M_PRODUCT 04/16/2021
MEDTRONIC SOFAMOR DANEK USA, INC T2 SPINAL SYSTEM 03/30/2021
MEDTRONIC SOFAMOR DANEK USA, INC T2 SPINAL SYSTEM 03/25/2021
SYNTHES GMBH UNK - CAGE/SPACERS: SYNCAGE 03/15/2021
SYNTHES GMBH UNK - CAGE/SPACERS: CERVIOS 03/15/2021
MEDTRONIC SOFAMOR DANEK USA, INC CLYDESDALE VBS 02/09/2021
SYNTHES GMBH UNK - CONSTRUCTS: SYNFIX EVOLUTION 01/22/2021
SYNTHES GMBH UNK - CONSTRUCTS: SYNFIX EVOLUTION 01/22/2021
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