ClearanceBrief
510(k) K170421 ยท NHA Abutment, Implant, Dental, Endosseous

ET Hybrid Abutment

ApplicantHiossen, Inc., Fariless Hills PA, US
DecisionSubstantially Equivalent, Jan 11, 2018
ReceivedFeb 13, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K170421

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.