ClearanceBrief
510(k) K010291 ยท DZE Implant, Endosseous, Root-Form

ITI DENTAL IMPLANT SYSTEM

ApplicantStraumann USA, Waltham MA, US
DecisionSubstantially Equivalent, May 10, 2001
ReceivedJan 31, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K010291

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.