510(k) K063248 ยท NDN Cement, Bone, Vertebroplasty
ARCUATE VERTEBRAL AUGMENTATION SYSTEM
| Applicant | Medtronic Sofamor Danek, Memphis TN, US |
| Decision | Substantially Equivalent, Mar 13, 2007 |
| Received | Oct 26, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063248
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.