510(k) K140563 ยท MQP Spinal Vertebral Body Replacement Device
LATERAL VBR SYSTEM
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Aug 7, 2014 |
| Received | Mar 5, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140563
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.