510(k) K133592 ยท DZE Implant, Endosseous, Root-Form
NEODENT IMPLANT SYSTEM, TITAMAX TI EX ACQUA AND TI DRIVE ACQUA, TITAMAX SMART EX ACQUA AND DRIVE SMART ACQUA, TITAMAX CM
| Applicant | Neodent USA, Inc., Andover MA, US |
| Decision | Substantially Equivalent, Aug 22, 2014 |
| Received | Nov 22, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133592
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.