510(k) K021791 ยท MQP Spinal Vertebral Body Replacement Device
VERTE-STACK SPINAL SYSTEM
| Applicant | Medtronic Sofamor Danek, Memphis TN, US |
| Decision | Substantially Equivalent, Aug 26, 2002 |
| Received | May 31, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021791
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.