510(k) K190229 ยท GWO Plate, Cranioplasty, Preformed, Alterable
Stryker PEEK Customized Cranial Implant Kit
| Applicant | Stryker, Portage MI, US |
| Decision | Substantially Equivalent, Jul 11, 2019 |
| Received | Feb 5, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190229
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.