510(k) K161442 · OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
NuVasive® CoRoent® Small Interlock System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Sep 28, 2016 |
| Received | May 25, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161442
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.