510(k) K160221 ยท DZE Implant, Endosseous, Root-Form
Implance Dental Implant System, Implance Dental Abutment System
| Applicant | Ags Medikal Urunleri Ith. Ihr. Tic. Ltd. Sti., Istanbul, TR |
| Decision | Substantially Equivalent, Sep 12, 2016 |
| Received | Jan 29, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160221
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.