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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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120 records meeting your search criteria returned- Product Code: KWL Product Problem: Break Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US ACTIS BROACH SZ 6 10/12/2020
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 8 10/08/2020
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 6 09/21/2020
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 5 09/16/2020
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 4 08/26/2020
OSTEOREMEDIES, LLC REMEDY SPECTRUM GV HIP 08/17/2020
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 9 06/26/2020
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 7 06/26/2020
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 6 06/26/2020
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 1 06/26/2020
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