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FDA 510(k) Applications Submitted by Epic Extremity, LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K172441
08/11/2017
EPIC Extremity Fracture Plate System
EPIC Extremity, LLC
K182991
10/29/2018
EPIC Extremity Fusion Plate System
EPIC Extremity, LLC
K163038
10/31/2016
EPIC Extremity Snap-Off Screw
EPIC EXTREMITY, LLC
K153333
11/19/2015
Epic Extremity Cannulated Screw System
Epic Extremity, LLC
K153340
11/19/2015
Epic Extremity Plate System
Epic Extremity, LLC
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