HTGClass IIImplant
Prosthesis, Knee, Hemi-, Patellar Resurfacing, Uncemented
Orthopedic · 21 CFR 888.3580
MDR events2,066All time
Recalls0All time
Registered firms1Currently listed
510(k) clearances2All time
Recent MDR events
2,066 adverse event reports on file
- AESCULAP VEGAOct 17, 2018MalfunctionB. Braun / Aesculap Implant Systems, Llc.MW5080669
- UNKNOWN KNEE PATELLAAug 2, 2018InjuryDepuy Orthopaedics Inc Us1818910-2018-65610
- COLLECT.NO.QAS KNEE IMPLANTS VEGAMar 23, 2018MalfunctionAesculap Implant Systems9610612-2018-00130
- COLLECT.NO.QAS KNEE IMPLANTS VEGAMar 23, 2018MalfunctionAesculap Implant Systems9610612-2018-00126
- COLLECT.NO.QAS KNEE IMPLANTS VEGAMar 23, 2018MalfunctionAesculap Implant Systems9610612-2018-00127
- TIBIAL INSERTOct 13, 2015InjuryDepuy/ SynthesMW5057152
- UNKNOWN DEPUY 32MM PATELLAAug 28, 2015InjuryDepuy Orthopaedics, Inc.1818910-2015-29275
- UNITED ORTHOPEDIC CORPORATIONAug 5, 2015MalfunctionUnited Orthopedic Corporation5020846
- UNKNOWN DEPUY 41MM PATELLAJul 21, 2015InjuryDepuy Orthopaedics, Inc.1818910-2015-26104
- NEXGEN COMPLETE KNEE SOLUTION POLY PATELLAApr 22, 2015ZimmerMW5042278
Event type breakdown
Injury1,886
Malfunction102
Other49
Unspecified27
Death2
Recalls
0 recall events for this product code
No recalls on file for this product code.
Registered firms
1 firms currently registered for this product code
510(k) clearances
2 clearances for this product code