ClearanceBrief
510(k) K182650 ยท HRS Plate, Fixation, Bone

Arzzt Distal Radius and Ulna System

ApplicantTruemed Group, LLC, The Woodlands TX, US
DecisionSubstantially Equivalent, Jun 10, 2019
ReceivedSep 24, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K182650

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.