FDA 510(k) Applications Submitted by Rebecca R. Homan

FDA 510(k) Number Submission Date Device Name Applicant
K200068 01/13/2020 Arthrex DynaNite K-Wire Arthrex Inc.
K210994 04/02/2021 Arthrex Beveled FT Screws Arthrex Inc.
K201677 06/19/2020 Arthrex Mesh Plates Arthrex Inc.
K203180 10/26/2020 Arthrex DynaNite Nitinol Staples Arthrex Inc.
K213644 11/18/2021 Arthrex Knotless Mini TightRopes Arthrex Inc.
K180118 01/16/2018 Arthrex NanoSuture Anchor Arthrex Inc.
K190287 02/11/2019 Arthrex DynaNite« PIP (Hammertoe) Implant Arthrex Inc.
K220839 03/23/2022 Arthrex Compression FT Pins Arthrex Inc.
K221031 04/07/2022 Arthrex DualCompression Hindfoot Fusion Nail Implant System Arthrex Inc.
K201235 05/07/2020 Arthrex MaxForce MTP Compression Plates and Screws Arthrex Inc.
K191326 05/16/2019 Arthrex Mini Comprehensive Fixation System û 1.4mm & 1.6mm Module Arthrex Inc.
K201522 06/08/2020 Arthrex Syndesmosis TightRope XP Buttress Plate Implant System Arthrex Inc.
K191651 06/20/2019 Arthrex Nano SwiveLock Suture Anchor Arthrex Inc.
K172052 07/06/2017 Arthrex DynaNite Nitinol Staple Arthrex Inc.
K182361 08/30/2018 Arthrex Compression FT Screws Arthrex Inc.
K193156 11/14/2019 Arthrex Mini Comprehensive Fixation System - 1.0mm Screws Arthrex Inc.
K173656 11/29/2017 Arthrex FibuLock Nail Arthrex, Inc.
K193345 12/03/2019 Arthrex DynaNite Compression Plate Arthrex Inc.
K183395 12/07/2018 Arthrex 2.5 mm Tenodesis Screw Arthrex Inc.
K203834 12/30/2020 Arthrex Patella SuturePlates Arthrex Inc.
K191344 05/20/2019 Arthrex Mini Comprehensive Fixation System û 2.0mm & 2.4mm Module Arthrex Inc.


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