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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience(MAUDE)
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9 records meeting your search criteria returned- Product Code: KXA Product Problem: Failure to Osseointegrate Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 11/19/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 11/13/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 10/29/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL AUGMENT 10/29/2019
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP FEMORAL STEM 09/27/2019
DEPUY INTERNATIONAL LTD. 8010379 PROXIMA STD OFFSET R SZ 6 08/03/2018
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 04/25/2016
DEPUY ORTHOPAEDICS INC US SROM*STM LG 36+8L 18X13X215L 12/16/2014
DEPUY INTERNATIONAL LTD. 8010379 TOTAL ASR FEM IMP SIZE 53 09/05/2014
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