K260240
- 510(k) number
- K260240
- Device name
- SYMPHONY Navigation Ready Instruments
- Applicant
- Medos International SARL CH
- Product code
- OLO — Orthopedic Stereotaxic Instrument
- Decision date
- 2026-03-27
- Date received
- 2026-01-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 3.2 MB · U.S. public domain
Also available from FDA: K260240.pdf
Official FDA record: K260240
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.