510(k) K203479 ยท HRS Plate, Fixation, Bone
ExtremiLOCK Lateral Ankle Fusion Plates
| Applicant | Osteomed, Addison TX, US |
| Decision | Substantially Equivalent, Feb 24, 2021 |
| Received | Nov 27, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203479
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.