510(k) K170126 · NKB Thoracolumbosacral Pedicle Screw System
NuVasive® Reline® 4.5-5.0 System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Mar 9, 2017 |
| Received | Jan 13, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170126
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.