K241942
- 510(k) number
- K241942
- Device name
- TriMed Bridge Plates
- Applicant
- TriMed, Inc. CA · US
- Product code
- HRS — Plate, Fixation, Bone
- Decision date
- 2024-09-17
- Date received
- 2024-07-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.7 MB · U.S. public domain
Also available from FDA: K241942.pdf
Official FDA record: K241942
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.