ClearanceBrief
510(k) K863680 ยท DZE Implant, Endosseous, Root-Form

IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS

ApplicantInterpore Intl., Irvine CA, US
DecisionSubstantially Equivalent, Oct 24, 1986
ReceivedSep 19, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K863680

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.