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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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56 records meeting your search criteria returned- Product Code: KXA Product Problem: Malposition of Device Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS, INC. UNKNOWN DEPUY SZ. 18X13 SROM STEM 03/02/2015
DEPUY ORTHOPAEDICS INC US AML LG STATURE 15.0MM 02/24/2015
DEPUY INTERNATIONAL LTD. 8010379 TOTAL ASR FEM IMP SIZE 43 01/06/2015
DEPUY INTERNATIONAL LTD. 8010379 DEPUY ASR XL FEM IMP SIZE 45 12/03/2014
DEPUY INTERNATIONAL LTD. 8010379 DEPUY ASR XL FEM IMP SIZE 47 11/24/2014
MICROPORT ORTHOPEDICS INC. CONSERVE(R) SUPER FINISH FEMORAL 11/10/2014
DEPUY INTERNATIONAL LTD - 8010379 TOTAL ASR FEM IMP SIZE 46 10/09/2014
DEPUY INTERNATIONAL LTD. 8010379 TOTAL ASR FEM IMP SIZE 53 09/04/2014
DEPUY INTERNATIONAL LTD. 8010379 TOTAL ASR FEM IMP SIZE 43 08/28/2014
DEPUY INTERNATIONAL LTD. 8010379 DEPUY ASR XL FEM IMP SIZE 45 08/21/2014
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