ClearanceBrief
510(k) K003271 ยท DZE Implant, Endosseous, Root-Form

MODIFICATION TO ITI DENTAL IMPLANT SYSTEM

ApplicantInstitut Straumann AG, Waltham MA, US
DecisionSubstantially Equivalent, Mar 20, 2001
ReceivedOct 18, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K003271

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.