510(k) K760334 ยท HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
PROSTEHSIS, TOTAL KNEE REPLACEMENT
| Applicant | Depuy, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 11, 1976 |
| Received | Jul 29, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760334
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.