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Abraham Mathews Vice President, Regulatory Affairs and Quality Assurance Mr. Mathews began his career in the medical device industry with the Ethicon Division of Johnson & Johnson. As manager of regulatory affairs, he was responsible for product approval activities in the U.S. including 510(k)s, IDEs, PMAs, and PMA supplements. During his tenure at Ethicon, Mr. Mathews was appointed as HIMA (AdvaMed) Management Fellow, representing the interests of all medical device divisions of J&J through the Health Industry Manufacturers Association. He later joined Independence Technology, a new startup within J&J and a maker of class III medical devices, as the director of Regulatory Affairs, Quality Assurance. Mr. Mathews then joined Provasis Therapeutics as Vice President, Regulatory Affairs and Quality Assurance. Provasis was a start up venture that developed a class III medical device for the treatment of aneurysms and arteriovenous malformations. Immediately before joining Coherex Medical, Mr. Mathews was Vice President, Regulatory Affairs for Boston Scientific with responsibility for their west coast businesses including electrophysiology, neurovascular, cardiac imaging, and vascular protection. Mr. Mathews has a Masters of Science degree in Horticulture from Rutgers University. |
MANAGEMENT TEAM
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Notice: The Coherex FlatStent EF PFO Closure System has been CE Marked and is currently distributed outside the U.S.A. and Japan by Abbott Vascular. It is not available for investigational use or for commercial distribution at this time in the U.S.A.
