510(k) K161497 ยท DZE Implant, Endosseous, Root-Form
Dental Implants and Abutments
| Applicant | Ditron Precision, Ltd., Netanya, IL |
| Decision | Substantially Equivalent, Oct 28, 2016 |
| Received | Jun 1, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161497
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.