ClearanceBrief
510(k) K100850 ยท DZE Implant, Endosseous, Root-Form

COWELL IMPLANT SYSTEM

ApplicantCowellmedi Co., Ltd., Brea CA, US
DecisionSubstantially Equivalent, Dec 20, 2010
ReceivedMar 26, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K100850

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.