ClearanceBrief
510(k) K072447 ยท DZE Implant, Endosseous, Root-Form

PENTABORN

ApplicantMediscitec, Inc., Littleton CO, US
DecisionSubstantially Equivalent, Feb 15, 2008
ReceivedAug 31, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K072447

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.