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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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28 records meeting your search criteria returned- Product Code: KRR Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
MAKO SURGICAL RESTORIS MULTICOMPARTMENTAL KNEE PROSTHE 10/21/2014
MAKO SURGICAL RESTORIS MULTICOMPARTMENTAL KNEE PROSTHE 09/23/2014
MAKO SURGICAL RESTORIS MULTICOMPARTMENTAL KNEE PROSTHE 09/23/2014
MAKO SURGICAL RESTORIS MULTICOMPARTMENTAL KNEE PROSTHE 09/19/2014
MAKO SURGICAL RESTORIS MULTICOMPARTMENTAL KNEE PROTHES 09/03/2014
MAKO SURGICAL RESTORIS MULTICOMPARTMENTAL KNEE PROSTHE 08/29/2014
MAKO SURGICAL RESTORIS MULTICOMPARTMENTAL KNEE PROSTHE 08/16/2014
STRYKER ORTHOPAEDICS-MAHWAH AVON PAT/FEM JOINT SML 04/16/2014
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