510(k) K173938 ยท DZE Implant, Endosseous, Root-Form
IS-III HActive Fixture
| Applicant | Neobiotech Co., Ltd., Seoul, KR |
| Decision | Substantially Equivalent, May 24, 2018 |
| Received | Dec 26, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173938
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.