510(k) K221928 · OLO Orthopedic Stereotaxic Instrument
ROSA® Knee System
| Applicant | Orthosoft D/B/A Zimmer Cas, Montreal, CA |
| Decision | Substantially Equivalent, Oct 4, 2022 |
| Received | Jul 1, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221928
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.