Micro Therapeutics Dba Ev3 Neurovascular is one of 19694 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Micro Therapeutics Dba Ev3 Neurovascular - FDA 510(k) Cleared Devices
Recent clearances: SOLITAIRE 2 REVASCULARIZATION DEVICE, SOLITAIRE FR REVASCULARIZATION DEVICE, HYPERGLIDE AND HYPERFORM OCCLUSION BALLOON SYSTEMS
3
Total
3
Cleared
0
Denied
Micro Therapeutics Dba Ev3 Neurovascular has 3 FDA 510(k) cleared medical devices. Based in Lrvine, US.
Historical record: 3 cleared submissions from 2010 to 2012. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Micro Therapeutics Dba Ev3 Neurovascular Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Micro Therapeutics Dba Ev3 Neurovascular
3 devices