K233172
- 510(k) number
- K233172
- Device name
- NextAR Spine Platform
- Applicant
- Medacta International S.A. CH
- Product code
- SBF — Orthopedic Augmented Reality
- Decision date
- 2024-04-24
- Date received
- 2023-09-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K233172.pdf
Official FDA record: K233172
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.