ClearanceBrief
510(k) K925483 ยท DZE Implant, Endosseous, Root-Form

BRANEMARK SYST. HAND INST. DIA 297 & SDIA 276

ApplicantNobelpharma USA, Inc., Chicago IL, US
DecisionSubstantially Equivalent, May 2, 1994
ReceivedOct 30, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K925483

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.