ClearanceBrief
510(k) K160850 ยท DZE Implant, Endosseous, Root-Form

Nucleoss Tpure Implant System

ApplicantSanlilar Tibbi Cihazlar Med. Kim.San.Tic.Ltd.Sti, Bolgesi Tekeli, TR
DecisionSubstantially Equivalent, Aug 4, 2017
ReceivedMar 28, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K160850

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.