510(k) K192403 ยท NDN Cement, Bone, Vertebroplasty
VK100 Percutaneous Vertebral Augmentation System
| Applicant | Bonwrx, Ltd., Lansing MI, US |
| Decision | Substantially Equivalent, Nov 8, 2019 |
| Received | Sep 3, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192403
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.