K250620
- 510(k) number
- K250620
- Device name
- KLS Martin Ixos System
- Applicant
- KLS Martin L.P. FL · US
- Product code
- HRS — Plate, Fixation, Bone
- Decision date
- 2025-08-15
- Date received
- 2025-02-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K250620.pdf
Official FDA record: K250620
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.