510(k) K172587 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Mecta-C with titanium markers and Mecta-C TiPEEK with titanium markers
| Applicant | Medacta International S.A., Castel San Pietro (Ch), CH |
| Decision | Substantially Equivalent, Sep 18, 2017 |
| Received | Aug 28, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K172587
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.