Neurology
ARVIS® Shoulder
Kico Knee Innovation Company Pty Ltd
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
- K243950
- Decision date
- January 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.
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