ClearanceBrief
510(k) K171757 ยท NHA Abutment, Implant, Dental, Endosseous

Straumann Screw Retained Abutments

ApplicantStraumann USA, LLC (On Behalf of Institut Straumann Ag), Andover MA, US
DecisionSubstantially Equivalent, Nov 27, 2017
ReceivedJun 14, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K171757

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.