510(k) K760744 ยท HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
TAVERNETTI-TENNANT
| Applicant | Cutter Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 7, 1976 |
| Received | Sep 30, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760744
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.