ClearanceBrief
510(k) K902929 ยท DZE Implant, Endosseous, Root-Form

DEVICE PART NUMBER SVD2, 3, 4 SPADE DRILL

ApplicantMinimatic Implant Technology, Deerfield Beach FL, US
DecisionSubstantially Equivalent, Nov 13, 1990
ReceivedJul 3, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K902929

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.