ClearanceBrief
510(k) K202912 ยท HRS Plate, Fixation, Bone

ARIX Ankle Distal Tibia System

ApplicantJeil Medical Corporation, Seoul, KR
DecisionSubstantially Equivalent, Oct 29, 2020
ReceivedSep 29, 2020
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K202912

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.