ClearanceBrief
510(k) K180360 ยท DZE Implant, Endosseous, Root-Form

OKTAGON Implant System

ApplicantHager& Meisinger GmbH, Neuss, DE
DecisionSubstantially Equivalent, May 10, 2018
ReceivedFeb 9, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K180360

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.