510(k) K140003 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
COROENT SMALL INTERBODY SYSTEM
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Apr 3, 2014 |
| Received | Jan 2, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140003
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.