510(k) K862136 ยท HSX Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer
MODIFIED WHITESIDE POSTERIOR STABILIZED TOTAL KNEE
| Applicant | Dow Corning Wright, Arlington TN, US |
| Decision | Substantially Equivalent, Jul 14, 1986 |
| Received | Jun 4, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862136
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.