ClearanceBrief
510(k) K171285 ยท HRS Plate, Fixation, Bone

ARIX Diaphysis System

ApplicantJeil Medical Corporation, Seoul, KR
DecisionSubstantially Equivalent, Jul 24, 2017
ReceivedMay 1, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K171285

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.