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Spectranetics Corp announces FDA clearance of peripheral laser atherectomy devices for In-Stent Restenosis

Wednesday, 23 Jul 2014 04:27pm EDT 

Spectranetics Corp:Receives U.S. Food and Drug Administration (FDA) 510(k) clearance of their peripheral atherectomy products, Turbo-Tandem and Turbo Elite, for treatment of in-stent restenosis (ISR).Clearance prompts a new standard of care in ISR treatment with improved clinical outcomes. 

Company Quote

0.24 +0.70%
26 Dec 2014