ClearanceBrief
510(k) K050586 ยท DZE Implant, Endosseous, Root-Form

LEONE IMPLANT SYSTEM

ApplicantLeone S.P.A., Irvine CA, US
DecisionSubstantially Equivalent, Feb 27, 2006
ReceivedMar 7, 2005
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K050586

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.