510(k) K173819 ยท DZE Implant, Endosseous, Root-Form
MyPlant II Implant System
| Applicant | Hager& Meisinger GmbH, Neuss, DE |
| Decision | Substantially Equivalent, Aug 9, 2018 |
| Received | Dec 18, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173819
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.