ClearanceBrief
510(k) K170135 ยท DZE Implant, Endosseous, Root-Form

TREFOIL System

ApplicantNobel Biocare AB, Goteborg, SE
DecisionSubstantially Equivalent, May 11, 2017
ReceivedJan 17, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K170135

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.