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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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115 records meeting your search criteria returned- Product Code: KWY Product Problem: Loss of Osseointegration Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 09/01/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL AUGMENT 08/25/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 08/25/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 08/17/2020
DEPUY ORTHOPAEDICS INC US S-ROM*SLEEVE PRX ZT HA 16F-XXL 08/17/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 07/31/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL AUGMENT 07/23/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 07/23/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL AUGMENT 07/14/2020
DEPUY INTERNATIONAL LTD - 8010379 G2 PRESS FIT STEM SZ6L 06/17/2020
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