510(k) K210247 ยท JDO Device, Fixation, Proximal Femoral, Implant
OsteoCentric Integrated Hip Fastener System
| Applicant | Osteocentric Technologies D.B.A. Osteocentric Trauma, Logan UT, US |
| Decision | Substantially Equivalent, Apr 30, 2021 |
| Received | Jan 29, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210247
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.