510(k) K243999 ยท HRS Plate, Fixation, Bone
TriMed Ankle Fixation System
| Applicant | TriMed, Inc., Santa Clarita TX, US |
| Decision | Substantially Equivalent, Mar 19, 2025 |
| Received | Dec 26, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243999
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.