510(k) K201981 ยท DZE Implant, Endosseous, Root-Form
Magicore System
| Applicant | Innobiosurg Co., Ltd., Daejeon, KR |
| Decision | Substantially Equivalent, Aug 27, 2020 |
| Received | Jul 16, 2020 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K201981
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.