510(k) K200312 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Tryptik Ti
| Applicant | Spineart, Plan Les Ouates, CH |
| Decision | Substantially Equivalent, Apr 6, 2020 |
| Received | Feb 6, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200312
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.