FDA 510(k) Applications Submitted by Extremity Medical, LLC.

FDA 510(k) Number Submission Date Device Name Applicant
K171018 04/05/2017 Axis Charcot Fixation System, 4.5 to 8.5mm Screw System Extremity Medical, LLC.
K191525 06/10/2019 KinematX Total Wrist Arthroplasty System Extremity Medical, LLC.
K212297 07/22/2021 Omni Foot and Ankle Plating System Extremity Medical, LLC.
K172260 07/27/2017 Omni Foot Plating System Extremity Medical, LLC.
K192592 09/20/2019 Axis Plating System Extremity Medical, LLC.
K133636 11/26/2013 EXTREMITY MEDICAL HAMMERTOE DEVICE EXTREMITY MEDICAL, LLC.
K211261 04/26/2021 Axis Charcot Fixation System Extremity Medical, LLC.
K201556 06/10/2020 Intraosseous Fixation System Extremity Medical, LLC.


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