510(k) K070483 ยท DZE Implant, Endosseous, Root-Form
LEONE MONOIMPLANT FOR O-RING OVERDENTURE
| Applicant | Leone S.P.A., Sesto, Fiorentino, IT |
| Decision | Substantially Equivalent, Apr 19, 2007 |
| Received | Feb 20, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070483
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.