510(k) K890044 ยท HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
BIOPRO ANATOMIC UNICOMPARTMENTAL KNEE
| Applicant | Biopro, Inc., Port Huron MI, US |
| Decision | Substantially Equivalent for Some Indications, Nov 6, 1989 |
| Received | Jan 5, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890044
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.