510(k) K080559 ยท DZE Implant, Endosseous, Root-Form
DIO SM IMPLANT SYSTEM
| Applicant | Dsi, Inc., Los Angeles CA, US |
| Decision | Substantially Equivalent, Oct 9, 2008 |
| Received | Feb 28, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080559
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.