510(k) K262618 ยท MRW System, Facet Screw Spinal Device
Arthrex Spine Compression FT Screw
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Sep 24, 2026 |
| Received | Jul 28, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K262618
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.