510(k) K252153 ยท MRW System, Facet Screw Spinal Device
FFX Facet Fixation System
| Applicant | Sc Medica, Strasbourg, FR |
| Decision | Substantially Equivalent, Oct 16, 2025 |
| Received | Jul 9, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K252153
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.