510(k) K150474 ยท NKG Posterior Cervical Screw System
NuVasive VuePoint II OCT System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Oct 21, 2015 |
| Received | Feb 23, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150474
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.