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BIOTRONIK Congratulates Endosense on the FDA IDE Approval of the TOCCASTAR Clinical Trial and First Patient Enrollment


1/13/2011 8:47:47 AM

(BUSINESS WIRE)--BIOTRONIK SE Co. & KG highlights two key milestones toward receiving premarket approval (PMA) of the TactiCath, a novel technology for treating atrial fibrillation (AF): FDA IDE (investigational device exemption) approval and the first patient enrollment of the TOCCASTAR (TactiCath Contact Force Ablation Catheter Study for Atrial Fibrillation) clinical trial.

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