510(k) K133327 ยท DZE Implant, Endosseous, Root-Form
SATURNO(TM) OVERDENTURE IMPLANT SYSTEM
| Applicant | Zest Anchors, LLC, San Diego CA, US |
| Decision | Substantially Equivalent, Jun 25, 2014 |
| Received | Oct 29, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133327
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.