510(k) K222778 ยท DZE Implant, Endosseous, Root-Form
Osstem Implant System
| Applicant | Osstem Implant Co., Ltd., Busan, KR |
| Decision | Substantially Equivalent, Sep 23, 2023 |
| Received | Sep 14, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222778
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.