Fed Regist. 2015 May 4;80(85):25226-30.
The Food and Drug Administration (FDA or the Agency) is republishing in its entirety a final order entitled ``Medical Devices; Physical Medicine Devices; Classification of the Powered Lower Extremity Exoskeleton'' that published in the Federal Register on February 24, 2015. FDA is republishing to correct an inadvertent omission of information. FDA is classifying the powered lower extremity exoskeleton into class II (special controls). The special controls that will apply to the device are identified in this order and will be part of the codified language for the powered lower extremity exoskeleton's classification. The Agency is classifying the device into class II (special controls) in order to provide a reasonable assurance of safety and effectiveness of the device.
美国食品药品监督管理局(FDA或该机构)正在重新发布一份完整的最终命令,题为“医疗器械;物理医学设备;动力下肢外骨骼的分类”,该命令于2015年2月24日发布在《联邦公报》上。FDA重新发布是为了纠正无意中遗漏的信息。FDA正在将动力下肢外骨骼归类为II类(特殊控制)。本命令确定了将适用于该设备的特殊控制措施,这些措施将成为动力下肢外骨骼分类的编纂语言的一部分。该机构将该设备归类为II类(特殊控制),以便合理保证该设备的安全性和有效性。