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Guidant Stent Approved in EU

The company gets clearance to market the Xience V stent system.

Medical-device maker



said regulators for the European Union nations approved its new stent earlier than had been expected.

Approval by the European Union allows Guidant to market its Xience V stent system as a treatment for coronary artery disease. The stent is used to prop open clogged arteries and is coated with everolimus, a drug that prevents reclogging. The device will be ready for launch in the second quarter, Guidant said Monday.

"This early approval represents a significant milestone in Guidant's drug-eluting stent program and demonstrates our ongoing commitment to advancing the field of cardiovascular therapy through innovative solutions," said John Capek, president of Guidant's vascular intervention business.

Guidant, which also manufactures pacemakers and defibrillators, has been under fire since thousands of its devices were recalled last year. The Indianapolis-based company

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agreed to be acquired by another stent maker,

Boston Scientific

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, following a bidding war with

Johnson & Johnson

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for the troubled company.

Guidant's shares fell $1.39 to $72.33 near the market close Monday. Shares of Boston Scientific were down 84 cents, or 3.8%, to $20.80.