ClearanceBrief
510(k) K042462 ยท DZE Implant, Endosseous, Root-Form

AMERICAN DENTAL IMPLANT

ApplicantAmerican Dental Implant Corporation, New Castle PA, US
DecisionSubstantially Equivalent, Sep 21, 2004
ReceivedSep 10, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K042462

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.