510(k) K050997 ยท MQP Spinal Vertebral Body Replacement Device
EXPANSE VERTEBRAL BODY REPLACEMENT DEVICE
| Applicant | Flexuspine, Inc., Tyler TX, US |
| Decision | Substantially Equivalent, Oct 7, 2005 |
| Received | Apr 20, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050997
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.