510(k) K925849 ยท DZE Implant, Endosseous, Root-Form
ZEST IMPLANT ANCHOR
| Applicant | Zest Anchors, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Nov 18, 1994 |
| Received | Nov 18, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925849
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.