Guidant stent gets FDA clearance

Interventional-device firm Guidant has received Food and Drug Administration clearance for a new carotid stent system designed to reduce the risk of stroke associated with carotid artery disease.

The RX Acculink carotid stent system and RX Accunet embolic protection system provide a minimally invasive alternative to conventional open carotid artery surgery for patients at high surgical risk, according to the Indianapolis-based firm.

High-risk patients indicated for carotid stenting with Guidant's devices include those with significant heart, kidney, or lung disease; recurrence of a blockage following a prior carotid surgery; or with difficult-to-access neck anatomy, the company said.

By AuntMinnie.com staff writers
September 1, 2004

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