ClearanceBrief
510(k) K934825 ยท DZE Implant, Endosseous, Root-Form

BRANEMARK SYSTEM

ApplicantNobelpharma USA, Inc., Chicago IL, US
DecisionSubstantially Equivalent, Aug 8, 1994
ReceivedOct 8, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K934825

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.