510(k) K230583 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Tryptik Ti
| Applicant | Spineart SA, Plan-Les-Ouates, CH |
| Decision | Substantially Equivalent, Mar 22, 2023 |
| Received | Mar 2, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K230583
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.