ClearanceBrief
510(k) K013798 ยท DZE Implant, Endosseous, Root-Form

PROSTHETIC ACCESSORIES TO THE ITI DENTAL IMPLANT SYSTEM

ApplicantInstitut Straumann AG, Waltham MA, US
DecisionSubstantially Equivalent, Dec 19, 2001
ReceivedNov 15, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K013798

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.