Tryton Medical, Inc. Meets Primary Endpoint In Pivotal Confirmatory Study Of Tryton Side Branch Stent In Treatment Of Coronary Bifurcation Lesions

DURHAM, N.C.--(BUSINESS WIRE)--Tryton Medical, Inc., the leading developer of stents designed to treat coronary bifurcation lesions, today announced results from the pivotal Tryton Confirmatory Study confirming the acceptable acute safety profile of the Tryton Side Branch Stent for the treatment of coronary bifurcation lesions in vessels appropriate for a =2.5mm stent. Results are being presented today as part of the Featured Clinical Research session at Transcatheter Cardiovascular Therapeutics (TCT), the annual scientific symposium of the Cardiovascular Research Foundation (CRF) being held in San Francisco, Calif.

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