510(k) K250679 ยท MRW System, Facet Screw Spinal Device
FFX Facet Fixation System
| Applicant | Sc Medica, Strasbourg, FR |
| Decision | Substantially Equivalent, Dec 4, 2025 |
| Received | Mar 6, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250679
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.