ClearanceBrief
510(k) K193401 ยท DZE Implant, Endosseous, Root-Form

Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE Implants

ApplicantAltatec GmbH, Wimsheim, DE
DecisionSubstantially Equivalent, Sep 29, 2020
ReceivedDec 6, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K193401

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.