510(k) K062931 ยท DZE Implant, Endosseous, Root-Form
IMPLUS IMPLANT SYSTEM
| Applicant | Leader Italia S.R.L., New York NY, US |
| Decision | Substantially Equivalent, Nov 28, 2007 |
| Received | Sep 28, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062931
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.