510(k) K964259 ยท JDO Device, Fixation, Proximal Femoral, Implant
SYNTHES (USA) DDHS/DCS SYSTEM MODIFICATION
| Applicant | Synthes (Usa), Paoli PA, US |
| Decision | Substantially Equivalent, Jan 9, 1997 |
| Received | Oct 25, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964259
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.