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Boston Scientific Submits Final Modules to FDA for Approval of Second-Generation Small Vessel and Long Lesion Stents
Date:2/5/2009

n Scientific remains the overall drug-eluting stent market leader in the United States, with a 49 percent share of the market in December. The Company released three major DES products in the United States in 2008 with the PROMUS(R) Everolimus-Eluting Coronary Stent, the TAXUS Express Atom Stent and the TAXUS Liberte Stent. The Company expects to launch its third-generation drug-eluting stents -- the TAXUS Element(TM) Paclitaxel-Eluting Coronary Stent and the PROMUS Element Everolimus-Eluting Coronary Stent -- in Europe later this year.

The TAXUS Liberte Atom, TAXUS Liberte Long, TAXUS Element and PROMUS Element stents are investigational devices and are restricted under U.S. law to investigational use only.

The PROMUS(R) Stent is a private-labeled XIENCE(TM) V Everolimus-Eluting Coronary Stent System manufactured by Abbott and distributed by Boston Scientific. XIENCE(TM) V is a trademark of the Abbott Laboratories group of companies.

Boston Scientific is a worldwide developer, manufacturer and marketer of medical devices whose products are used in a broad range of interventional medical specialties. For more information, please visit: www.bostonscientific.com.

Cautionary Statement Regarding Forward-Looking Statements

This press release contains forward-looking statements within the meaning of Section 21E of the Securities Exchange Act of 1934. Forward-looking statements may be identified by words like "anticipate," "expect," "project," "believe," "plan," "estimate," "intend" and similar words. These forward-looking statements are based on our beliefs, assumptions and estimates using information available to us at the time and are not intended to be guarantees of future events or performance. These forward-looking statements include, among other things, statements regarding regulatory approvals,
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