510(k) K230180
K230180 is an FDA 510(k) premarket notification submitted by Orthosoft Inc (D/B/A Zimmer Cas) for the device "Rosa Knee System". The FDA issued a decision of Substantially Equivalent on February 22, 2023. The device falls under product code OLO (Orthopedic Stereotaxic Instrument), 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
- February 22, 2023
- Date Received
- January 23, 2023
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Orthopedic Stereotaxic Instrument
- Device Class
- Class II
- Regulation Number
- 882.4560
- Review Panel
- OR
- Submission Type
Stereotaxic guidance during orthopedic surgery procedures. Indicated for Orthopedic joint or spine surgery. Neurological stereotaxic instruments are classified under product code HAW.