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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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114 records meeting your search criteria returned- Product Code: NPJ Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
MAKO SURGICAL CORP. MCK FEMORAL-LM-RL-SZ 3 01/05/2017
MAKO SURGICAL CORP. MCK FEMORAL-RM-LL-SZ 2 06/26/2016
MAKO SURGICAL CORP. MCK TIBIAL ONLAY INSERT-SZ 2-8MM 06/17/2016
STRYKER ORTHOPAEDICS-MAHWAH AVON PAT/FEM JOINT MED 05/06/2016
MAKO SURGICAL CORP. MCK TIBIAL ONLAY INSERT-SZ 5-9MM 12/16/2015
MAKO SURGICAL CORP. MCK TIBIAL ONLAY INSERT-SZ 6-8MM 11/24/2015
CONFORMIS, INC. IDUO G2 10/07/2015
STRYKER ORTHOPAEDICS-MAHWAH SCORPIO U-DOME PATELLA 10/06/2015
CONFORMIS I DUO G2 07/07/2015
CONFORMIS IDUO G2 03/18/2015
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