510(k) K012473 ยท DZE Implant, Endosseous, Root-Form
VIDENT HEXTOP, SYNOCTA IN-CERAM BLANK/COPING MANUFACTURED BY VIDENT
| Applicant | Vident, Brea CA, US |
| Decision | Substantially Equivalent, Sep 11, 2002 |
| Received | Aug 2, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012473
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.