Home » Truvic Gets FDA’s 510(k) Clearance for its Prodigy Thrombectomy System
Truvic Gets FDA’s 510(k) Clearance for its Prodigy Thrombectomy System
Campbell, Calif.-based Truvic Medical has received 510(k) clearance from the FDA for its Prodigy thrombectomy system for the removal of blood clots from inside a peripheral artery or vein.
The Prodigy system, which is the company’s first thrombectomy system to gain the FDA’s clearance, enables the removal of blood clots in a single session without the use of thrombolytics.
Truvic Medical is a subsidiary of Imperative Care, which is focused on stroke intervention and peripheral thrombectomy products.
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