ClearanceBrief
510(k) K062129 ยท DZE Implant, Endosseous, Root-Form

P.0004 IMPLANTS

ApplicantInstitut Straumann AG, Andover MA, US
DecisionSubstantially Equivalent, Oct 20, 2006
ReceivedJul 26, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K062129

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.