510(k) K945028 ยท KRO Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
FINN KNEE SYSTEM
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent for Some Indications, Feb 14, 1996 |
| Received | Oct 13, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K945028
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.