ClearanceBrief
510(k) K152158 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

ARIX Ankle System

ApplicantJeil Medical Corporation, Seoul, KR
DecisionSubstantially Equivalent, Sep 28, 2015
ReceivedAug 3, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K152158

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.