ClearanceBrief
510(k) K953435 ยท DZE Implant, Endosseous, Root-Form

BRANEMARK RADIOGRAPHIC DEPTH GUAGE

ApplicantNobelpharma USA, Inc., Westmont IL, US
DecisionSubstantially Equivalent, Oct 3, 1995
ReceivedJul 21, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K953435

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.