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Augmedics’ xvision system registration method gains FDA clearance
Augmedics has received the Food and Drug Administration (FDA) 510(k) clearance of the new CT-to-fluoroscopy (CT-Fluoro) registration method for its xvision spine system. Navigating off using ...
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Clinical trial requirements
Clinical investigations may also meet the FDA definition of “applicable clinical trial,” in which case they must follow the agency’s trial registration and results reporting requirements. There are ...
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Augmedics picks up FDA nod for new CT-Fluoro registration
Augmedics announced today that the FDA cleared the CT-to-fluoroscopy (CT-Fluoro) registration method for its xvision Spine System.