510(k) K072660 ยท DZE Implant, Endosseous, Root-Form
ENDURE IMPLANT, MODEL 5108, 5111, 5113, 5114
| Applicant | Imtec Corp., Ardmore OK, US |
| Decision | Substantially Equivalent, Dec 12, 2007 |
| Received | Sep 21, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072660
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.