510(k) K182974 ยท NKB Thoracolumbosacral Pedicle Screw System
NuVasive Reline System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Feb 13, 2019 |
| Received | Oct 26, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182974
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.