510(k) K190322 · ODP Intervertebral Fusion Device With Bone Graft, Cervical
SCARLET® AC-T Secured Anterior Cervical Cage
| Applicant | Spineart, Plan Les Ouates, CH |
| Decision | Substantially Equivalent, Mar 4, 2019 |
| Received | Feb 13, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K190322
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.