510(k) K242933 ยท OLO Orthopedic Stereotaxic Instrument
SPINEART Navigation Instrument System
| Applicant | Spineart SA, Plan Les Ouates, CH |
| Decision | Substantially Equivalent, Jun 18, 2025 |
| Received | Sep 25, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242933
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.