510(k) K954856 ยท JDN Implant, Fixation Device, Spinal
CANNULATED FEMORAL NAIL
| Applicant | Synthes (Usa), Paoli PA, US |
| Decision | Substantially Equivalent, Mar 8, 1996 |
| Received | Oct 23, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954856
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.