510(k) K052261 ยท MQP Spinal Vertebral Body Replacement Device
MODIFICATION TO: VERTE-STACK SPINAL SYSTEM
| Applicant | Medtronic Sofamor Danek USA, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Oct 7, 2005 |
| Received | Aug 19, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K052261
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.