510(k) K171938 ยท PML Bone Cement, Posterior Screw Augmentation
KYPHON Xpede Bone Cement, CD HORIZON Fenestrated Screw Set
| Applicant | Medtronic, Memphis TN, US |
| Decision | Substantially Equivalent, Oct 23, 2017 |
| Received | Jun 28, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171938
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.