K232533
- 510(k) number
- K232533
- Device name
- ROSA Partial Knee System
- Applicant
- Orthosoft D/B/A Zimmer Cas CA
- Product code
- OLO — Orthopedic Stereotaxic Instrument
- Decision date
- 2023-11-16
- Date received
- 2023-08-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K232533.pdf
Official FDA record: K232533
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.