510(k) K781608 ยท HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
CENTRAL PEG TIBIAL COMPONENT
| Applicant | Howmedica Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 27, 1978 |
| Received | Sep 18, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781608
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.