510(k) K230180 ยท OLO Orthopedic Stereotaxic Instrument
Rosa Knee System
| Applicant | Orthosoft Inc (D/B/A Zimmer Cas), Montreal, CA |
| Decision | Substantially Equivalent, Feb 22, 2023 |
| Received | Jan 23, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K230180
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.