510(k) K180498 ยท PML Bone Cement, Posterior Screw Augmentation
NuVasive Reline Fenestrated Screws, High V+ Bone Cement
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Nov 28, 2018 |
| Received | Feb 26, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180498
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.