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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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89 records meeting your search criteria returned- Product Code: KWY Product Problem: Nonstandard Device Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
DEPUY INTERNATIONAL LTD. ¿ 8010379 UNIDENTIFIED ASR HEAD 02/18/2016
DEPUY INTERNATIONAL LTD - 8010379 DEPUY ASR XL FEM IMP SIZE 46 01/21/2016
DEPUY INTERNATIONAL LTD. ¿ 8010379 LARGE MOD HEAD ADAPT 12/14 +5 12/18/2015
DEPUY INTERNATIONAL LTD - 8010379 LARGE MOD HEAD ADAPT 12/14 +5 12/03/2015
DEPUY INTERNATIONAL LTD - 8010379 DEPUY ASR XL FEM IMP SIZE 45 10/26/2015
DEPUY INTERNATIONAL LTD.8010379 LARGE MOD HEAD ADAPT 12/14 +5 08/17/2015
DEPUY DEPUY HEAD 02/25/2014
STRYKER ORTHOPAEDICS CORK ABGII MODULAR LONG NECK 02/18/2014
STRYKER ORTHOPAEDICS CORK ABG11 MODULAR LONG NECK 01/28/2014
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