510(k) K161923 ยท DZE Implant, Endosseous, Root-Form
J2A SLA Dental Implant System
| Applicant | Kj Meditech Co., Ltd., Gwangju, KR |
| Decision | Substantially Equivalent, Nov 9, 2017 |
| Received | Jul 13, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161923
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.