SILVER SPRING, MD – Boston Scientific is voluntarily recalling two core wires for its Rotablator Rotational Atherectomy System, according to an alert from the US Food and Drug Administration (FDA) [1] ...

PARIS, France—A novel atherectomy system designed to clear away hard plaque components may improve outcomes in patients with severely calcified coronary lesions compared with historical controls, ...

November 11, 2011 (San Francisco, California) — Rotational atherectomy prior to the implantation of a drug-eluting stent (DES) failed to have any impact on in-stent late lumen loss in elderly patients ...

Please provide your email address to receive an email when new articles are posted on . In patients with severely calcified coronary lesions, planned rotational atherectomy appears to be a safe ...

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 — ...

Calcified femoropopliteal arterial disease remains a major challenge in endovascular therapy. Vessel preparation technologies have emerged to improve ...

The FDA today granted PMA approval to the Diamondback 360 Coronary Orbital Atherectomy System (OAS) for the treatment of severely calcified coronary arteries. Cardiovascular Systems, the manufacturer ...

The Gibraltar Cardiac Association has presented a rotablator device to the Gibraltar Health Authority for use in heart ...