510(k) K033926 ยท MQP Spinal Vertebral Body Replacement Device
HOURGLASS VERTEBRAL BODY SPACER
| Applicant | Medtronic Sofamor Danek, Memphis TN, US |
| Decision | Substantially Equivalent, Jul 7, 2004 |
| Received | Dec 18, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033926
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.