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

virtual 3D com base em dados CT de um paciente específico. O modelo virtual pode, então, ser utilizado com a finalidade de simular, analisar e avaliar as opções pré-operatórias de tratamento cirúrgico, antes de se efetuar o procedimento real, o que pode aumentar a confiança do médico no procedimento real. Uma vez que o modelo 3D foi exportado para o ambiente de simulação ANGIO Mentor™, o médico pode praticar inúmeras vezes para avaliar diferentes técnicas, utilizando ferramentas e implantes realistas.

A Sociedade de Cirurgia Vascular sugere que os cirurgiões realizem um mínimo de 100 diagnósticos, 50 intervenções e 10 casos de TEVAR para se tornar certificado. Com esta nova aplicação inovadora, os médicos podem realmente receber treinamento prático em procedimentos TEVAR, incluindo a implantação precisa de stents simples e múltiplos, bem como reparo de balonamento, antes de operar um paciente vivo. O PRS simplifica o planejamento do procedimento e oferece uma solução abrangente para o treinamento e simulação de procedimentos específicos de paciente destinados a melhorar o nível profissional de médicos experientes e novos.

Segundo a Dra. Yael Friedman , diretora de Assuntos Regulatórios da Simbionix, o histórico da Simbionix de proporcionar aos profissionais de saúde ferramentas de simulação inovadoras é a base de mais um produto de sucesso. "A correção de aneurisma torácico endovascular é um dos procedimentos mais avançados médicos realizados pelos cirurgiões endovasculares. A Simbionix está extremamente satisfeita por ter recebido o autorização da FDA e orgulhosa de nossa nova aplicação clínica
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SOURCE Simbionix USA Corporation
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