Medical Device Manufacturer · IE , Galway

Neuravi, Ltd. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2018

Recent clearances: EmboTrap II Revascularization Device, EMBOTRAP III Revascularization Device, EMBOTRAP III Revascularization Device, EMBOTRAP III Revascularization Device

4
Total
4
Cleared
0
Denied

FDA 510(k) Regulatory Record - Neuravi, Ltd. Neurology ✕

4 devices
1-4 of 4
Cleared Oct 13, 2021
EmboTrap II Revascularization Device, EMBOTRAP III Revascularization Device
K212908 · NRY
Neurology · 30d
Cleared Jul 30, 2021
EMBOTRAP III Revascularization Device
K211338 · NRY
Neurology · 88d
Cleared Jul 14, 2020
EMBOTRAP III Revascularization Device
K193063 · NRY
Neurology · 253d
Cleared CT May 09, 2018
EmboTrap ll Revascularization Device
K173452 · NRY
Neurology · 184d
Filters
Filter by Specialty
All4 Neurology 4