510(k) K040422 ยท MQP Spinal Vertebral Body Replacement Device
MODIFICATION TO VERTE-STACK
| Applicant | Medtronic Sofamor Danek, Memphis TN, US |
| Decision | Substantially Equivalent, Mar 19, 2004 |
| Received | Feb 18, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K040422
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.