FDA 510(k) Applications Submitted by Ryan Kenney

FDA 510(k) Number Submission Date Device Name Applicant
K160641 03/07/2016 Solitaire Platinum Revascularization Device, 6x40 mm Micro Therapeutics, Inc. d/b/a ev3 Neurovascular
K180705 03/19/2018 Riptide Aspiration System React 68 Catheter Micro Therapeutics, Inc. d/b/a ev3 Neurovascular
K180715 03/19/2018 React 68 Catheter Micro Therapeutics, Inc. d/b/a ev3 Neurovascular
K181186 05/03/2018 Solitare Platinum Revascularization Device Micro Therapeutics, Inc. d/b/a ev3 Neurovascular
K161879 07/08/2016 Solitaire Platinum Revascularization Device Micro Therapeutics, Inc. d/b/a ev3 Neurovascular
K182097 08/03/2018 React 71 Catheter Micro Therapeutics, Inc. d/b/a ev3 Neurovascular
K182101 08/03/2018 Riptide Aspiration System (React 71 Catheter) Micro Therapeutics, Inc. d/b/a ev3 Neurovascular
K172448 08/14/2017 Riptide Aspiration System Micro Therapeutics, Inc., d/b/a ev3 Neurovascular
K213435 10/22/2021 MAGIC Flow-Dependent Microcatheter Balt USA, LLC
K193548 12/20/2019 Mirage Hydrophilic Guidewire, X-pedion Hydrophilic Guidewire Micro Therapeutics, Inc. d/b/a ev3 Neurovascular
K223929 12/30/2022 LagunaÖ Clot Retriever System and MalibuÖ Aspiration Catheter System (Laguna Thrombectomy System) Innova Vascular, Inc.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact