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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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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 ORTHOPAEDICS, INC. LCS COMPLETE FEM POR R STD 03/11/2015
DEPUY ORTHOPAEDICS, INC. LCS COMP RP INSERT STD 12.5MM 03/11/2015
DEPUY ORTHOPAEDICS, INC. 1818910 MBT POR TIBIAL TRAY SZ2.5 03/11/2015
DEPUY IRELAND 9616671 MBT POR KEEL TIB TRAY SZ4 03/09/2015
DEPUY IRELAND 9616671 ATTUNE RP TIB BASE SZ 3 CEM 03/03/2015
DEPUY IRELAND 9616671 MBT CEM TIBIAL TRAY SZ2.5 02/10/2015
DEPUY IRELAND 9616671 LCS COMPLETE FEM CEM R STD 02/05/2015
DEPUY IRELAND 9616671 MBT CEM TIBIAL TRAY SZ3 02/05/2015
DEPUY IRELAND 9616671 MBT CEM KEEL TIB TRAY SZ2.5 01/12/2015
DEPUY ORTHOPAEDICS, INC. 1818910 LCS COMPLETE M/B PAT POR LG 12/03/2014
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