ClearanceBrief
510(k) K181703 ยท DZE Implant, Endosseous, Root-Form

Straumann BLX Line Extension - Implants, SRAs and Anatomic Abutments

ApplicantInstitut Straumann AG, Basel, CH
DecisionSubstantially Equivalent, Dec 28, 2018
ReceivedJun 27, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K181703

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.