ClearanceBrief
510(k) K170780 ยท HRS Plate, Fixation, Bone

ARIX Foot System (2.3/2.8)

ApplicantJeil Medical Corporation, Seoul, KR
DecisionSubstantially Equivalent, Aug 14, 2017
ReceivedMar 15, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K170780

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.