ClearanceBrief
510(k) K925772 ยท DZE Implant, Endosseous, Root-Form

BRANEMARK SYSTEM GUIDE PINS

ApplicantNobelpharma USA, Inc., Chicago IL, US
DecisionSubstantially Equivalent, Sep 16, 1993
ReceivedNov 16, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K925772

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.