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Terceira aprovação da FDA para produto revolucionário Simbionix
Date:3/29/2013

CLEVELAND, 29 de março de 2013 /PRNewswire/ -- A Simbionix USA Corporation, fornecedora líder mundial em educação médica e treinamento por simulação, recebeu autorização da FDA para sua aplicação TEVAR (correção de aneurisma torácico endovascular) para o PROcedure Rehearsal Studio™ (PRS). Esta aplicação se junta à família do PRS autorizado para aplicações de marketing para intervenção em carótidas e procedimentos EVAR (correção de aneurisma endovascular).

(Logo: http://photos.prnewswire.com/prnh/20120502/529202-a)

A TEVAR é uma modalidade de tratamento emergente, que foi rapidamente acolhida por médicos que tratam de doenças da aorta torácica. É uma abordagem muito menos invasiva do que a cirurgia aberta. Além disso, a disponibilidade e facilidade relativa da aplicação com a TEVAR mudaram e ampliaram as opções de tratamento de doenças da aorta torácica, inclusive em pacientes considerados inadequados à cirurgia aberta. As habilidades necessárias para realizar a TEVAR exigem dedicado treinamento formal, porque este procedimento requer consideráveis ​​exigências perceptivas, cognitivas e psicomotoras dos cirurgiões.

O PROcedure Rehearsal Studio utiliza a tecnologia revolucionária, desenvolvida pela Simbionix, permitindo aos médicos ensaiar um procedimento endovascular completo em um modelo anatômico
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SOURCE Simbionix USA Corporation
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