510(k) K262032 ยท HRS Plate, Fixation, Bone
TriMed Non-Spanning Wrist Fusion Plates (NSFL-STD);TriMed Non-Spanning Wrist Fusion Plates (NSFR-STD);TriMed Non-Spanning Wrist Fusion Plates (NSFL-SHB );TriMed Non-Spanning Wrist Fusion Plates (NSFR-SHB )
| Applicant | TriMed, Inc., Santa Clarita CA, US |
| Decision | Substantially Equivalent, Jul 16, 2026 |
| Received | Jun 17, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K262032
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.