510(k) K960617 ยท HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
ADVANCE TIBIAL COMPONENT
| Applicant | Wrightmedicaltechnologyinc, Arlington TN, US |
| Decision | Substantially Equivalent for Some Indications, May 8, 1996 |
| Received | Feb 13, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960617
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.