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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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69 records meeting your search criteria returned- Product Code: KWY Product Problem: Malposition of Device Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS, INC. UNKNOWN DEPUY FEMORAL STEM 02/24/2015
DEPUY ORTHOPAEDICS, INC. UNKNOWN DEPUY SZ. 54 PINNACLE CUP 02/18/2015
DEPUY ORTHOPAEDICS, INC. UNKNOWN DEPUY FEMORAL STEM 02/06/2015
ENCORE MEDICAL, L.P. FOUNDATION HIP 01/08/2015
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN DEPUY ACETABULAR CUP 12/12/2014
DEPUY ORTHOPAEDICS INC US SROM STM STD 36+12L 17X22 12/04/2014
DEPUY ORTHOPAEDICS INC US PINNACLE SECTOR II CUP 50MM 06/23/2014
DEPUY ORTHOPAEDICS, INC.1818910 UNKNOWN DEPUY EXCEL FEMORAL HIP STEM 04/10/2014
DEPUY ORTHOPAEDICS, INC. PINNACLE SECTOR II CUP 50MM 02/04/2014
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