ClearanceBrief
510(k) K101913 ยท DZE Implant, Endosseous, Root-Form

ANTHOFIT OI, ANTHOFIT HE, OSSFIT AND AXIOM

ApplicantAnthogyr Sas, Sallanches, FR
DecisionSubstantially Equivalent, Mar 11, 2011
ReceivedJul 8, 2010
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K101913

DateFirm and productCodeLinked 510(k)
Sep 8, 2016Anthogyr
Axiom REG implants Sterile The Axiom REG implants are used as artificial root structures for replacement of missing teeth. They can be used for stabilization of removable prostheses or fixation of si
Terminated
DZENone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.