510(k) K113779 ยท DZE Implant, Endosseous, Root-Form
CONELOG IMPLANT SYSTEM
| Applicant | Altatec GmbH, San Diego CA, US |
| Decision | Substantially Equivalent, Dec 14, 2012 |
| Received | Dec 22, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113779
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.