510(k) K934162 ยท JDO Device, Fixation, Proximal Femoral, Implant
PROFORM HA HIP SYSTEM
| Applicant | Stelkast Company, Pittsburgh PA, US |
| Decision | Substantially Equivalent for Some Indications, Mar 9, 1994 |
| Received | Aug 27, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934162
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.