510(k) K012681 ยท DZE Implant, Endosseous, Root-Form
ANKYLOS
| Applicant | Dentsply Ceramco, Burlington NJ, US |
| Decision | Substantially Equivalent, Aug 22, 2003 |
| Received | Aug 14, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012681
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.