510(k) K170961 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
NuVasive CoRoent Small Interlock II System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Jun 8, 2017 |
| Received | Mar 31, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170961
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.