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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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