510(k) K240699 · OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
SCARLET® AC-Ti
| Applicant | Spineart SA, Plan-Les-Ouates, CH |
| Decision | Substantially Equivalent, May 10, 2024 |
| Received | Mar 14, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240699
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.