510(k) K043226 ยท DZE Implant, Endosseous, Root-Form
ENDURE IMPLANT, MODELS 3508, 4308, 3520, 4320
| Applicant | Imtec Corp., Ardmore OK, US |
| Decision | Substantially Equivalent, Jan 13, 2005 |
| Received | Nov 22, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K043226
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.