510(k) K180198 · NKG Posterior Cervical Screw System
NuVasive® VuePoint® II OCT System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Mar 15, 2018 |
| Received | Jan 24, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180198
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.