510(k) K801524 ยท DZE Implant, Endosseous, Root-Form
ZEST PLANT
| Applicant | Zest Anchors, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Jul 21, 1980 |
| Received | Jul 1, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801524
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.