Clearance Summary
ROSA Partial Knee System received FDA 510(k) clearance under submission number K232533, sponsored by Orthosoft D/B/A Zimmer Cas. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2023-11-16.
- Submission: K232533
- Applicant / Sponsor: Orthosoft D/B/A Zimmer Cas
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.4560
- Decision date: 2023-11-16
Classification & Regulation
This clearance is catalogued under FDA product code OLO and 21 CFR 882.4560, within the Neurology review panel as a Class II device.