510(k) K041509 ยท DZE Implant, Endosseous, Root-Form
ANKYLOS DENTAL IMPLANT SYSTEM
| Applicant | Friadent GmbH, Lake Forest CA, US |
| Decision | Substantially Equivalent, Aug 26, 2004 |
| Received | Jun 7, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041509
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.