510(k) K172065 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
SCARLET AC-T
| Applicant | Spineart, Plan Les Ouates, CH |
| Decision | Substantially Equivalent, Sep 29, 2017 |
| Received | Jul 7, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172065
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.