510(k) K080129 ยท DZE Implant, Endosseous, Root-Form
SECURE IMPLANT SYSTEM (2.5/3.0MM)
| Applicant | Dio Department Dsi, Inc., Los Angeles CA, US |
| Decision | Substantially Equivalent, May 30, 2008 |
| Received | Jan 17, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080129
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.