Penumbra's Revolutionary PE Treatment Trial Hits 100-Patient Mark, Results Could Transform Blood Clot Care
6 Articles
6 Articles
Penumbra completes enrolment in trial for pulmonary embolism
Penumbra has completed subject enrolment in the multi-centre, randomised controlled trial, STORM-PE, for pulmonary embolism (PE).The post Penumbra completes enrolment in trial for pulmonary embolism appeared first on Medical Device Network.
Aventus thrombectomy system gains FDA clearance for PE treatment - Interventional News
Inquis Medical has announced that its Aventus thrombectomy system has received 510(k) clearance from the US Food and Drug Administration (FDA) for an expanded indication to treat pulmonary embolism (PE). The Aventus System is a next-generation mechanical thrombectomy platform developed in close collaboration with physicians to address critical limitations of current technologies. “The FDA’s clearance of the Aventus system marks a major milestone…
Aventus thrombectomy system gains FDA clearance for PE treatment - Cardiovascular News
Inquis Medical has announced that its Aventus thrombectomy system has received 510(k) clearance from the US Food and Drug Administration (FDA) for an expanded indication to treat pulmonary embolism (PE). The Aventus System is a next-generation mechanical thrombectomy platform developed in close collaboration with physicians to address critical limitations of current technologies. “The FDA’s clearance of the Aventus system marks a major milestone…
Penumbra, Inc. Announces Completion of Enrollment for Landmark STORM-PE Randomized Controlled Trial
STORM-PE is a first-of-its-kind clinical trial comparing computer assisted vacuum thrombectomy (CAVT™) using Penumbra's Lightning Flash™ with anticoagulation versus anticoagulation alone in the treatment of acute intermediate-high risk pulmonary embolism
Coverage Details
Bias Distribution
- There is no tracked Bias information for the sources covering this story.
To view factuality data please Upgrade to Premium