510(k) K173975 ยท DZE Implant, Endosseous, Root-Form
UF(II) Wide Fixture
| Applicant | Dio Corporation, Busan, KR |
| Decision | Substantially Equivalent, Jun 1, 2018 |
| Received | Dec 29, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173975
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.