ClearanceBrief
510(k) K053354 ยท DZE Implant, Endosseous, Root-Form

INTERMEZZO PLUS FIXTURE

ApplicantMegagen Co., Ltd., Santa Fe Springs CA, US
DecisionSubstantially Equivalent, Apr 13, 2006
ReceivedDec 2, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K053354

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.