K250865
- 510(k) number
- K250865
- Device name
- KLS Martin IPS Forearm System
- Applicant
- KLS-Martin L.P. FL · US
- Product code
- HRS — Plate, Fixation, Bone
- Decision date
- 2025-11-14
- Date received
- 2025-03-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K250865.pdf
Official FDA record: K250865
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.