510(k) K020264 ยท HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
REPICCI II UNICONDYLAR KNEE SYSTEM
| Applicant | Biomet Orthopedics, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Feb 8, 2002 |
| Received | Jan 25, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K020264
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.