Biomaterials, Medical Devices and Tissue Engineering: An Integrated Approach
Frederick H. Silver
Broschiertes Buch

Biomaterials, Medical Devices and Tissue Engineering: An Integrated Approach

An integrated approach

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are then selected and must meet the general 'biocompatibility' require ments. Prototypes are built and tested to include biocompatibility evalua tions based on ASTM standard procedures. The device is validated for sterility and freedom from pyrogens before it can be tested on animals or humans. Medical devices are classified as class I, II or III depending on their invasiveness. Class I devices can be marketed by submitting notification to the FDA. Class II and III devices require either that they show equivalence to a device marketed prior to 1976 or that they receive pre-marketing approval. ...