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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 US UNKNOWN HIP FEMORAL STEM 11/14/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 11/14/2019
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP FEMORAL STEM 08/09/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 08/08/2019
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP FEMORAL STEM 08/02/2019
MICROPORT ORTHOPEDICS INC. CONSERVE(R) SUPER FINISH FEMORAL 06/06/2018
DEPUY INTERNATIONAL LTD - 8010379 SROM 9/10 18X12X135 36 01/19/2018
MICROPORT ORTHOPEDICS INC. CONSERVE(R) SUPER FINISH FEMORAL 09/29/2017
DEPUY INTERNATIONAL LTD. 8010379 DEPUY ASR XL FEM IMP SIZE 46 11/22/2016
DEPUY INTERNATIONAL LTD. 8010379 TOTAL ASR FEM IMP SIZE 46 06/24/2016
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