510(k) K262184 · JDO Device, Fixation, Proximal Femoral, Implant
GANNET®
| Applicant | BAAT Medical Products B.V., Hengelo, NL |
| Decision | Substantially Equivalent, Oct 22, 2026 |
| Received | Jun 29, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K262184
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.