ClearanceBrief
510(k) K161989 ยท NHA Abutment, Implant, Dental, Endosseous

PREMIUM Implant Systems SHELTA Implant Systems

ApplicantSweden & Martina S.P.A., Due Carrare, IT
DecisionSubstantially Equivalent, Feb 1, 2018
ReceivedJul 19, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K161989

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.