510(k) K191553 · NKG Posterior Cervical Screw System
NuVaisve® Reline® Cervical System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Aug 14, 2019 |
| Received | Jun 12, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191553
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.