Home » FDA APPROVES NESS DEVICE FOR PARALYZED LEGS
FDA APPROVES NESS DEVICE FOR PARALYZED LEGS
Medical device company NESS Neuromuscular Electrical Stimulation Systems Ltd. announced that it received US Food and Drug Administration (FDA) approval to market its NESS L300 device for moving paralyzed legs in the US. Globes Online (http://www.globes.co.il/serveen/globes/DocView.asp?did=1000139240&fid=1279)
KEYWORDS FDAnews Device Daily Bulletin
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