K243623
- 510(k) number
- K243623
- Device name
- SpineAR SNAP (SyncAR Spine)
- Applicant
- Surgical Theater, Inc. OH · US
- Product code
- SBF — Orthopedic Augmented Reality
- Decision date
- 2024-12-24
- Date received
- 2024-11-25
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 2.4 MB · U.S. public domain
Also available from FDA: K243623.pdf
Official FDA record: K243623
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.