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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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