510(k) K071033 ยท MQP Spinal Vertebral Body Replacement Device
T2 XVBR SPINAL SYSTEM
| Applicant | Medtronic Sofamor Danek, Memphis TN, US |
| Decision | Substantially Equivalent, Aug 14, 2007 |
| Received | Apr 12, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071033
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.