510(k) K021621 ยท HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
FIXED BEARING UNI COMPONENT
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jun 5, 2002 |
| Received | May 16, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K021621
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.