FDA 510(k) Applications Submitted by TRUEMED GROUP LLC

FDA 510(k) Number Submission Date Device Name Applicant
K200575 03/05/2020 TRUEMED HAND, FOOT AND ANKLE PLATES SYSTEM TRUEMED GROUP LLC
K172189 07/20/2017 Ins Hilden Humeral Arzzt, Ins Hilden Cannulated Tibial Arzzt, Ins Hilden Femoral Arzzt & Ins Hilden Retrograde Femoral Arzzt Truemed Group LLC
K182650 09/24/2018 Arzzt Distal Radius and Ulna System Truemed Group LLC


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