ClearanceBrief
510(k) K042354 ยท DZE Implant, Endosseous, Root-Form

MODIFICATION TO: CRESCO TI IMPLANT CONCEPT

ApplicantCresco TI Systems AB, Kristianstad, SE
DecisionSubstantially Equivalent, Sep 21, 2004
ReceivedAug 30, 2004
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K042354

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.