ClearanceBrief
510(k) K161177 ยท DZE Implant, Endosseous, Root-Form

Axiom PX

ApplicantAnthogyr Sas, Sallanches, FR
DecisionSubstantially Equivalent, Jun 15, 2017
ReceivedApr 26, 2016
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K161177

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.