ClearanceBrief
510(k) K131066 ยท DZE Implant, Endosseous, Root-Form

AXIOM REG

ApplicantAnthogyr Sas, Sallanches, FR
DecisionSubstantially Equivalent, Feb 21, 2014
ReceivedApr 16, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K131066

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.