510(k) K170271 ยท MQP Spinal Vertebral Body Replacement Device
NuVasive(r) Monolith Corpectomy System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Mar 30, 2017 |
| Received | Jan 27, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170271
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.