510(k) K230243 · OLO Orthopedic Stereotaxic Instrument
ROSA® Knee System
| Applicant | Orthosoft D/B/A Zimmer Cas, Montreal, CA |
| Decision | Substantially Equivalent, Mar 29, 2023 |
| Received | Jan 30, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230243
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.