510(k) K140051 ยท DZE Implant, Endosseous, Root-Form
KJ EXTERNAL IMPLANT SYSTEM
| Applicant | Kj Meditech Co., Ltd., Fullerton CA, US |
| Decision | Substantially Equivalent, Oct 30, 2014 |
| Received | Jan 9, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140051
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.