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. |
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