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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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136 records meeting your search criteria returned- Product Code: KXA Patient Problem: Limited Mobility Of The Implanted Joint Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
BIOMET UK LTD. RECAP RESURFACING SYSTEM FEMORAL HEAD 02/28/2017
BIOMET UK LTD. RECAP RESURFACING SYSTEM FEMORAL HEAD 02/28/2017
DEPUY INTERNATIONAL LTD. 8010379 UNKNOWN DEPUY ASR XL HEAD 01/25/2017
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN DEPUY FEMORAL STEM 12/11/2016
DEPUY INTERNATIONAL LTD. 8010379 UNKNOWN DEPUY ASR XL HEAD 11/23/2016
DEPUY INTERNATIONAL LTD. 8010379 UNKNOWN DEPUY ASR XL HEAD 08/02/2016
DEPUY INTERNATIONAL LTD. 8010379 UNKNOWN DEPUY ASR XL HEAD 07/14/2016
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN DEPUY STEM 07/14/2016
DEPUY INTERNATIONAL LTD. 8010379 UNKNOWN DEPUY ASR XL HEAD 07/14/2016
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN DEPUY STEM 07/14/2016
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