510(k) K150362 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
NuVasive CoRoent Small Interbody System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Jun 11, 2015 |
| Received | Feb 12, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150362
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.