510(k) K163032 ยท NDN Cement, Bone, Vertebroplasty
Kyphon Xpede Bone Cement
| Applicant | Medtronic, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Feb 27, 2017 |
| Received | Oct 31, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163032
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.