K262032
- 510(k) number
- K262032
- Device name
- 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. CA · US
- Product code
- HRS — Plate, Fixation, Bone
- Decision date
- 2026-07-16
- Date received
- 2026-06-17
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K262032.pdf
Official FDA record: K262032
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.