510(k) K202393 ยท NDN Cement, Bone, Vertebroplasty
SpineJack Expansion Kit
| Applicant | Stryker Corporation, Portage MI, US |
| Decision | Substantially Equivalent, Oct 20, 2020 |
| Received | Aug 21, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202393
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.