510(k) K070569 ยท DZE Implant, Endosseous, Root-Form
SM INTERNAL./EXTERNAL IMPLANT SYSTEM
| Applicant | Dio Department Dsi, Inc., Santa Fe Springs CA, US |
| Decision | Substantially Equivalent, Nov 8, 2007 |
| Received | Feb 28, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070569
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.