510(k) K923613 ยท JDO Device, Fixation, Proximal Femoral, Implant
SYNTHES LIMITED CONTACT-DYNAMIC HIP SCREW IMPLANT
| Applicant | Synthes (Usa), Paoli PA, US |
| Decision | Substantially Equivalent, Jun 22, 1993 |
| Received | Jul 21, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923613
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.