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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
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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 IRELAND - 9616671 ACTIS BROACH SZ 7 02/20/2019
DEPUY IRELAND 9616671 ACTIS BROACH SZ 6 02/01/2019
DEPUY IRELAND 9616671 ACTIS BROACH SZ 5 02/01/2019
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 9 01/16/2019
DEPUY IRELAND 9616671 ACTIS BROACH SZ 5 12/28/2018
DEPUY ORTHOPAEDICS INC US ACTIS REAMER SZ 4 AND 5 11/30/2018
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 5 11/14/2018
DEPUY FRANCE SAS 3003895575 CORAIL2 STD SIZE 12 11/01/2018
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 4 10/11/2018
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 4 08/21/2018
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