510(k) K030639 ยท DZE Implant, Endosseous, Root-Form
XIVE 3.0 DENTAL IMPLANT SYSTEM
| Applicant | Friandent GmbH, Lake Forest CA, US |
| Decision | Substantially Equivalent, Aug 12, 2003 |
| Received | Feb 28, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030639
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.