510(k) K230567
K230567 is an FDA 510(k) premarket notification submitted by Orthosoft Inc (D/B/A Zimmer Cas) for the device "OptiVu ROSA® MxR". The FDA issued a decision of Substantially Equivalent on June 13, 2023. The device falls under product code SBF (Orthopedic Augmented Reality), a Class II device regulated under 21 CFR 882.4560. Orthosoft Inc (D/B/A Zimmer Cas) has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 13, 2023
- Date Received
- March 1, 2023
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Orthopedic Augmented Reality
- Device Class
- Class II
- Regulation Number
- 882.4560
- Review Panel
- OR
- Submission Type
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.