Neurology
SpineAR SNAP (SyncAR Spine)
Surgical Theater, Inc.
FDA
FDA-cleared AI medical device
An orthopedic augmented reality device provides visual guidance during orthopedic procedures, where the use of stereotaxic navigation is utilized. Visual guidance is displayed as augmented reality stereoscopic images to intraoperatively augment the users field of view.
FDA Submission Metadata
- Submission number
- K252054
- Decision date
- September 2025
- FDA panel
- Neurology
- Product code
- SBF
This entry is sourced from the FDA AI/ML-Enabled Medical Devices list. No editorial review yet — the catalogue may add a deeper review of this device in future.
Regulatory Approvals
FDA
US FDA 510k
K252054
This entry is on our editorial review queue. Full evaluation — performance metrics, clinical evidence, safety record — lands as our review pipeline graduates each device. The information above is what's been verified to date.