Penumbra has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for Thunderbolt, a computer-assisted vacuum thrombectomy system for acute ischemic stroke.
Thunderbolt introduces modulated aspiration to the company's neuro thrombectomy portfolio. The system is designed to detect, loosen, and remove clots at the site of occlusion, according to the company. Penumbra said Thunderbolt is the first such system to deliver modulated aspiration for stroke.
Modulated aspiration may facilitate more consistent and complete clot removal when used in conjunction with standard aspiration thrombectomy catheters, according to the company. The system will be prepackaged with one of four of Penumbra’s RED catheters, Penumbra noted.



















