ClearanceBrief
510(k) K022859 ยท DZE Implant, Endosseous, Root-Form

ABUTMENT AND PROSTHETIC ACCESSORIES TO THE ITI DENTAL IMPLANT SYSTEM

ApplicantStraumann USA, Waltham MA, US
DecisionSubstantially Equivalent, Sep 19, 2002
ReceivedAug 28, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K022859

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.