Bioness, Valencia, California, announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market a smaller leg cuff for use with the company’s functional electrical stimulation (FES) L300® Foot Drop System. The new cuff size provides access to the L300 for patients with smaller calf sizes.
Magnets Are Newest Prosthetic Control Method
A research team from the Scuola Superiore Sant’Anna has developed the first prosthesis with magnetic control, a new way of...
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