510(k) K100976 ยท MQP Spinal Vertebral Body Replacement Device
T2 XVBR 1.5 SPINAL SYSTEM
| Applicant | Medtronic Sofamor Danek USA, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Oct 21, 2010 |
| Received | Apr 8, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100976
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.