510(k) K030243 ยท DZE Implant, Endosseous, Root-Form
ENDURE IMPLANT, MODEL 3508,3511,3514,4308,4311,4314
| Applicant | Imtec Corp., Ardmore OK, US |
| Decision | Substantially Equivalent, Apr 23, 2003 |
| Received | Jan 23, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030243
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.