Artio Medical Receives FDA Clearance for Solus Gold™ Embolization Device
PRAIRIE VILLAGE, Kan., March 22, 2022 /PRNewswire/ -- Artio Medical, Inc., a medical device company developing innovative products for the peripheral vascular, neurovascular, and cardiology markets, today announced it received US Food and Drug Administration (FDA) clearance for its Solus Gold Embolization Device, a next-generation product for peripheral vascular occlusion.
- PRAIRIE VILLAGE, Kan., March 22, 2022 /PRNewswire/ -- Artio Medical, Inc. , a medical device company developing innovative products for the peripheral vascular, neurovascular, and cardiology markets, today announced it received US Food and Drug Administration (FDA) clearance for its Solus GoldEmbolization Device, a next-generation product for peripheral vascular occlusion.
- The Solus Gold Embolization Device is indicated to obstruct or reduce the rate of blood flow in the peripheral vasculature.
- Artio Medical is a medical device company committed to developing innovative products for the treatment of peripheral vascular, neurovascular, and cardiology diseases.
- The Solus Gold Embolization Device combines a flexible catheter assembly and a non-porous, balloon-like gold implant for easy delivery, precise placement, and immediate vessel occlusion.