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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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142 records meeting your search criteria returned- Product Code: NJL Product Problem: Malposition of Device Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
DEPUY IRELAND 9616671 ATTUNE RP TIB BASE SZ 9 CEM 03/21/2019
DEPUY IRELAND 9616671 ATTUNE RP TIB BASE SZ 4 CEM 03/04/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN KNEE TIBIAL TRAY 11/16/2018
DEPUY IRELAND 9616671 ATTUNE PS FEM RT SZ 7 CEM 10/17/2018
DEPUY IRELAND 961610 ATTUNE RP TIB BASE SZ 5 CEM 09/07/2018
DEPUY IRELAND - 9616671 ATTUNE RP TIB BASE SZ 8 CEM 07/03/2018
DEPUY IRELAND - 9616671 ATTUNE RP TIB BASE SZ 6 CEM 06/29/2018
DEPUY IRELAND 9616671 ATTUNE RP TIB BASE SZ 8 CEM 06/26/2018
DEPUY IRELAND - 9616671 ATTUNE RP TIB BASE SZ 4 CEM 06/21/2018
DEPUY ORTHOPAEDICS INC US MBT CEM KEEL TIB TRAY SZ2 05/23/2018
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