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ATS Medical Announces Fourth Quarter and Full Year 2009 Results
Date:3/1/2010

  • The Company expects to receive regulatory approval for an additional valve repair product in the second quarter of 2010.  The additional product represents further expansion of the Company's annuloplasty repair product portfolio to meet broader clinical applications.  

Surgical Cryoablation

  • The Company has completed protocol development and will begin selecting investigation sites for the CryoMaze study, a prospective, multi-center clinical study of its CryoMaze cryoablation products to study the safety and efficacy of the use of the products for the treatment of atrial fibrillation.  The study will have one year follow-up with interim data points to validate the safety and efficacy of the CryoMaze products used to create the lesions of the gold-standard Cox-Maze III lesion sets.  This is the first and only multicenter study to mandate the Cox-Maze III lesion set for the treatment of atrial fibrillation with an energy source.


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SOURCE ATS Medical, Inc.
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