ClearanceBrief
510(k) K152836 ยท DZE Implant, Endosseous, Root-Form

TREFOIL System

ApplicantNobel Biocare AB, Goteborg, SE
DecisionSubstantially Equivalent, Apr 11, 2016
ReceivedSep 29, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K152836

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.