ClearanceBrief
510(k) K173141 ยท DZE Implant, Endosseous, Root-Form

CSM Submerged3-L Implant System

ApplicantCsm Implant, Daegu, KR
DecisionSubstantially Equivalent, Sep 19, 2018
ReceivedSep 29, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K173141

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.