510(k) K151651 ยท PLR Spinal Vertebral Body Replacement Device - Cervical
NuVasive X-CORE Mini Cervical Expandable VBR System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Sep 25, 2015 |
| Received | Jun 18, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151651
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.