510(k) K091883 ยท MQP Spinal Vertebral Body Replacement Device
T2 SPINAL SYSTEM
| Applicant | Medtronic Sofamor Danek USA, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Sep 21, 2009 |
| Received | Jun 24, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091883
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.