510(k) K252807 ยท HRS Plate, Fixation, Bone
Arthrex Anatomic Lapidus Plates and I-Beam Lapidus Plates
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Jan 12, 2026 |
| Received | Sep 3, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K252807
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.