K241893
- 510(k) number
- K241893
- Device name
- CROSSNAV Navigation Enabled Instruments and UNAS Navigation Arrays
- Applicant
- Medos International SARL CH
- Product code
- OLO — Orthopedic Stereotaxic Instrument
- Decision date
- 2024-09-16
- Date received
- 2024-06-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K241893.pdf
Official FDA record: K241893
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.