510(k) K151167 ยท MQP Spinal Vertebral Body Replacement Device
NuVasive PEEK Corpectomy System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Sep 3, 2015 |
| Received | May 1, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151167
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.