510(k) K011406 ยท MQP Spinal Vertebral Body Replacement Device
SPINAL MESH SYSTEM
| Applicant | Medtronic Sofamor Danek, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Dec 27, 2001 |
| Received | May 8, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011406
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.