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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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15 records meeting your search criteria returned- Product Code: KXA Product Problem: Patient-Device Incompatibility Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
DEPUY PINNACLE SECTOR 2 ACETABULAR CUP&ULTRAME 10/30/2015
MICROPORT ORTHOPEDICS INC. CONSERVE(R) SUPER FINISH FEMORAL 05/28/2015
BIOMET ORTHOPEDICS RECAP CEMENT FMRL HD RESUR 42M 01/14/2015
MICROPORT ORTHOPEDICS INC. CONSERVE(R) SUPER FINISH FEMORAL 11/10/2014
DEPUY INTERNATIONAL LTD. 8010379 DEPUY ASR XL FEM IMP SIZE 46 08/27/2014
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