ClearanceBrief
510(k) K091701 ยท NHA Abutment, Implant, Dental, Endosseous

STRAUMANN MODIFIED DENTAL ABUTMENT

ApplicantInstitut Straumann AG, Andover MA, US
DecisionSubstantially Equivalent, Dec 22, 2009
ReceivedJun 10, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K091701

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.