510(k) K230195 ยท OLO Orthopedic Stereotaxic Instrument
Neo ADVISE software
| Applicant | Comerge AG, Zurich, CH |
| Decision | Substantially Equivalent, Mar 8, 2024 |
| Received | Jan 25, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230195
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.