510(k) K083805 ยท DZE Implant, Endosseous, Root-Form
ANKYLOS C/X DENTAL IMPLANT SYSTEM
| Applicant | Dentsply Intl., Inc., York PA, US |
| Decision | Substantially Equivalent, May 22, 2009 |
| Received | Dec 22, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083805
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.