ClearanceBrief
510(k) K002614 ยท DZE Implant, Endosseous, Root-Form

ADVENT IMPLANT SYSTEM

ApplicantCore-Vent Corp., Las Vegas NV, US
DecisionSubstantially Equivalent, Dec 8, 2000
ReceivedAug 22, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K002614

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.