ClearanceBrief
510(k) K081419 ยท DZE Implant, Endosseous, Root-Form

STRAUMANN DENTAL IMPLANT SYSTEM

ApplicantInstitut Straumann AG, Andover MA, US
DecisionSubstantially Equivalent, Feb 20, 2009
ReceivedMay 20, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K081419

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.