510(k) K140347 ยท DZE Implant, Endosseous, Root-Form
ANKYLOS C/X IMPLANT SYSTEM
| Applicant | Dentsply Intl., Inc., York PA, US |
| Decision | Substantially Equivalent, Aug 20, 2014 |
| Received | Feb 11, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140347
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.