ClearanceBrief
510(k) K953774 ยท DZE Implant, Endosseous, Root-Form

BRANEMARK RESTORATIVE INSTRUMENT & COMPONENT TRAY

ApplicantNobelpharma USA, Inc., Westmont IL, US
DecisionSubstantially Equivalent, Sep 27, 1995
ReceivedAug 14, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K953774

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.