ClearanceBrief
510(k) K090377 ยท DZE Implant, Endosseous, Root-Form

SINUS QUICK EB SYSTEM

ApplicantNeobiotech Co., Ltd., Santa Fe Springs CA, US
DecisionSubstantially Equivalent, Aug 28, 2009
ReceivedFeb 17, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K090377

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.