ClearanceBrief
510(k) K190040 ยท NHA Abutment, Implant, Dental, Endosseous

Straumann BLX Line Extension - New Abutments

ApplicantInstitut Straumann AG, Basel, CH
DecisionSubstantially Equivalent, Apr 8, 2019
ReceivedJan 8, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K190040

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.