FDA 510(k) Applications Submitted by ORTHOPEDIC DESIGNS NORTH AMERICA, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K210146 01/21/2021 Cannulated Compression Device System Orthopedic Designs North America, Inc.
K152295 08/13/2015 Talon DistalFix Antegrade/Retrograde Femoral Nail ORTHOPEDIC DESIGNS NORTH AMERICA, INC.
K173255 10/10/2017 Talon DistalFix Humeral Nail Orthopedic Designs North America, Inc.
K111352 05/13/2011 TALON DISTALFIX PROXIMAL FEMORAL NAIL ORTHOPEDIC DESIGNS NORTH AMERICA, INC.


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