FDA Authorizes VR Treatment for Chronic Lower Back Pain
Clinical studies of AppliedVR's EaseVRx showed a 30% reduction in patients' pain.
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Clinical studies of AppliedVR's EaseVRx showed a 30% reduction in patients' pain.
Fact-Checked The FDA made several moves in April, from lifting the pause on the J&J vaccine to recalls on certain pills and vitamins. Bakhtiar Zein/iStock COVID-Related News The CDC and FDA have lifted the pause of the Johnson & Johnson vaccine following a complete review of rare blood clots. Following a thorough safety review — including two meetings of the Centers for Disease Control and Prevention's (CDC) Advisory Committee on Immunization Practices — the U.S. Food and Drug Administration (FDA) and the CDC issued a statement on April 23 saying that the recommended pause regarding the...
FDA Authorizes Marketing of Device to Facilitate Muscle Rehabilitation in Stroke Patients News provided by Share this article Share this article SILVER SPRING, Md., April 23, 2021 /PRNewswire/ -- Today, the U.S. Food and Drug Administration authorized marketing of a new device indicated for use in patients 18 and older undergoing stroke rehabilitation to facilitate muscle re-education and for maintaining or increasing range of motion. The Neurolutions IpsiHand Upper Extremity Rehabilitation System (IpsiHand System) is a Brain-Computer-Interface (BCI) device that assists in rehabilitation for ...
FDA authorizes marketing of a new device for use in patients undergoing stroke rehabilitation Today, the U.S. Food and Drug Administration authorized marketing of a new device indicated for use in patients 18 and older undergoing stroke rehabilitation to facilitate muscle re-education and for maintaining or increasing range of motion. The Neurolutions IpsiHand Upper Extremity Rehabilitation System (IpsiHand System) is a Brain-Computer-Interface (BCI) device that assists in rehabilitation for stroke patients with upper extremity—or hand, wrist and arm—disability. Thousands of stroke surviv...