Micro Therapeutics, Inc. d/b/a ev3 Neurovascular is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Micro Therapeutics, Inc. d/b/a ev3 Neurovascular - FDA 510(k) Cleared...
Recent clearances: Rist 079 Radial Access Guide Catheter, Riptide™ Aspiration Pump, Riptide Aspiration System
32
Total
32
Cleared
0
Denied
Micro Therapeutics, Inc. d/b/a ev3 Neurovascular has 32 FDA 510(k) cleared neurology devices. Based in Lrvine, US.
Latest FDA clearance: Jan 2025. Active since 2014.
Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Inneuroco, Inc. as regulatory consultant. 4 devices have linked clinical trials registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Micro Therapeutics, Inc. d/b/a ev3 Neurovascular
32 devices
Cleared
Jan 02, 2025
Rist 079 Radial Access Guide Catheter
Neurology
232d
Cleared
Dec 02, 2024
Riptide™ Aspiration Pump
General & Plastic Surgery
28d
Cleared
Oct 29, 2024
Riptide Aspiration System
Neurology
29d
Cleared
Jul 27, 2021
Rist 071 Radial Access Guide Catheter
Neurology
29d
Cleared
Jul 07, 2021
Axium Detachable Coil
Neurology
226d
Cleared
CT
Mar 01, 2021
Solitaire X Revascularization Device
Neurology
105d
Cleared
Feb 09, 2021
Concerto Versa, Detachable Coil
Cardiovascular
134d
Cleared
CT
Nov 20, 2020
Solitaire Platinum Revascularization Device, Solitaire X Revascularization...
Neurology
333d
Cleared
Sep 14, 2020
Marathon Flow Directed Micro Catheter
Neurology
28d
Cleared
Jul 21, 2020
Riptide Aspiration System
Neurology
29d
Cleared
Jul 21, 2020
Mirage Hydrophilic Guidewire
Neurology
29d
Cleared
Jan 18, 2020
Mirage Hydrophilic Guidewire, X-pedion Hydrophilic Guidewire
Neurology
29d