510(k) K211238 ยท NDN Cement, Bone, Vertebroplasty
SpineJack Expansion Kit, Vertaplex Radiopaque Bone Cement, Vertaplex HV Radiopaque Bone Cement
| Applicant | Stryker Instruments, Portage MI, US |
| Decision | Substantially Equivalent, Jun 25, 2021 |
| Received | Apr 26, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211238
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.