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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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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

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ManufacturerBrand NameDate Report Received
MICROPORT ORTHOPEDICS INC. CONSERVE(R) SUPER FINISH FEMORAL 11/03/2017
MICROPORT ORTHOPEDICS INC. CONSERVE(R) SUPER FINISH FEMORAL 11/03/2017
ZIMMER BIOMET, INC. RECAP CEMENT FMRL HD RESUR 58M 11/02/2017
DEPUY INTERNATIONAL LTD. 8010379 DEPUY ASR XL FEM IMP SIZE 49 10/30/2017
MICROPORT ORTHOPEDICS INC. CONSERVE(R) SUPER FINISH FEMORAL 10/27/2017
MICROPORT ORTHOPEDICS INC. CONSERVE(R) SUPER FINISH FEMORAL 10/27/2017
DEPUY IRELAND¿ 9616671 UNKNOWN DEPUY SROM HEAD 28MM 10/27/2017
DEPUY INTERNATIONAL LTD.8010379 TOTAL ASR FEM IMP SIZE 51 10/26/2017
DEPUY INTERNATIONAL LTD. - 8010379 TOTAL ASR FEM IMP SIZE 46 10/26/2017
DEPUY INTERNATIONAL LTD - 8010379 DEPUY ASR XL FEM IMP SIZE 47 10/26/2017
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