K233513
- 510(k) number
- K233513
- Device name
- Remex Spine Surgery Navigation System II
- Applicant
- Remex Medical Corp. TW
- Product code
- OLO — Orthopedic Stereotaxic Instrument
- Decision date
- 2024-05-01
- Date received
- 2023-11-01
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K233513.pdf
Official FDA record: K233513
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.