510(k) K162694 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Ayers Rock Cervical interbody fusion system
| Applicant | Spineway, Ecully, FR |
| Decision | Substantially Equivalent, Jan 12, 2017 |
| Received | Sep 27, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162694
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.