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Edwards Lifesciences

This article was originally published in The Gray Sheet

Executive Summary

Next-generation Lifepath endovascular graft system for abdominal aortic aneurysms, which uses stronger "wireform" supports, gains CE mark approval for European marketing. In April 2000, Edwards suspended sales of a first-generation system outside the U.S., as well as clinical trials worldwide, following fractures in the wire scaffolding

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