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Tech Vasc Interv Radiol ; 23(1): 100661, 2020 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-32192636

RESUMO

Medical devices can help patients lose weight. The Food and Drug Administration (FDA) Center for Devices and Radiological Health is responsible for assuring the safety and effectiveness of devices used for weight loss. Interventional radiologists may conduct clinical studies of devices for weight loss, such as embolization beads to stop blood flow to gastric arteries or cryoablation systems to ablate metabolism-linked nerves. The purposes of this paper are (1) to clarify the FDA's role providing regulatory oversight of clinical studies of medical devices; (2) to explain how to engage with the FDA; and (3) to provide information on the design of clinical studies intended to support a weight loss indication. In particular, Investigational Device Exemptions (IDEs) are needed for significant risk studies for new devices, or for off-label use of legally marketed devices. The FDA is available through the Pre-Submission process to assist when determining if a study requires an IDE, and to discuss plans for submitting an IDE. The FDA works with medical device manufacturers and clinical researchers who want to bring novel weight-loss devices to market.


Assuntos
Cirurgia Bariátrica/instrumentação , Aprovação de Equipamentos , Embolização Terapêutica/instrumentação , Obesidade/terapia , Radiografia Intervencionista/instrumentação , United States Food and Drug Administration , Redução de Peso , Cirurgia Bariátrica/efeitos adversos , Embolização Terapêutica/efeitos adversos , Desenho de Equipamento , Humanos , Obesidade/diagnóstico , Obesidade/fisiopatologia , Segurança do Paciente , Radiografia Intervencionista/efeitos adversos , Medição de Risco , Fatores de Risco , Resultado do Tratamento , Estados Unidos
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