ClearanceBrief
510(k) K092542 ยท DZE Implant, Endosseous, Root-Form

M

ApplicantMediscitec, Inc., Greenwood Village CO, US
DecisionSubstantially Equivalent, Apr 23, 2010
ReceivedAug 19, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K092542

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.