Please provide your email address to receive an email when new articles are posted on . Other tools for interventional cardiologists have come and gone, but atherectomy technology has persisted and — ...

October 9, 2007 — The US Food and Drug Administration (FDA) has granted 510(k) clearance to a peripheral atherectomy device for the treatment of peripheral artery disease, a prothrombin time test for ...

WASHINGTON, DC, UNITED STATES, October 30, 2025 /EINPresswire.com/ -- The CardioVascular Coalition (CVC) today commended the publication of a landmark paper providing ...

ST. PAUL, Minn.--(BUSINESS WIRE)-- Cardiovascular Systems, Inc. (CSI®) (NASDAQ: CSII), a medical device company developing and commercializing innovative interventional treatment systems for patients ...

A final option, less commonly used, is a technique called atherectomy. This treatment uses a device that cuts or grinds away the hardened deposition (atheroma) within the artery. Atherectomy is less ...

ST. PAUL, Minn.--(BUSINESS WIRE)--Cardiovascular Systems, Inc. (NASDAQ:CSII) (CSI), today announced that it has received FDA clearance for its new ViperWire Advance ® Peripheral Guide Wire with Flex ...

Please provide your email address to receive an email when new articles are posted on . The FDA has cleared a 225 cm radial access catheter for PAD atherectomy. Radial access may reduce bleeding risk ...

CONSHOHOCKEN, Pa.--(BUSINESS WIRE)--Rex Medical, L.P., a medical device design and development company, today announced that it has received 510k Clearance from the U.S. Food and Drug Administration ...

ProPublica reporters are looking into the booming business around peripheral artery disease, a condition that afflicts 6.5 million Americans over age 40. It’s caused when fatty plaque builds up in a ...

ViperWire Advance Peripheral Guide Wire with Flex Tip Offers Greater Flexibility and Navigation; Improves Systems’ Ease-of-Use When Treating Calcified Lesions in Torturous Arterial Anatomy ST. PAUL, ...