510(k) K230764 ยท JDO Device, Fixation, Proximal Femoral, Implant
OsteoCentric Integrated Hip Fastener System
| Applicant | OsteoCentric Technologies, Logan UT, US |
| Decision | Substantially Equivalent, Apr 18, 2023 |
| Received | Mar 20, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K230764
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.