FDA 510(k) Applications Submitted by J. Doug Patterson

FDA 510(k) Number Submission Date Device Name Applicant
K191118 04/26/2019 Avanti Distal Radius and Forearm System Avanti Orthopaedics, Inc.
K211592 05/24/2021 Avanti Orthopaedics Ulnar Shortening System Avanti Orthopaedics, Inc.
K222967 09/27/2022 Avanti Orthopaedics 2.2mm and 2.7mm Cannulated Screws, Avanti Orthopaedics 3.2mm and 4.0mm Cannulated Screws Avanti Orthopaedics, Inc.


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