ClearanceBrief
510(k) K994119 ยท DZE Implant, Endosseous, Root-Form

SYNOCTA ANGLED ABUTMENTS

ApplicantStraumann USA, Waltham MA, US
DecisionSubstantially Equivalent, Mar 17, 2000
ReceivedDec 6, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K994119

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.