510(k) K173148 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
ACIF
| Applicant | Coligne AG, Zurich, CH |
| Decision | Substantially Equivalent, Dec 1, 2017 |
| Received | Sep 29, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173148
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.