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See today's BioWorld MedTech
Home » Wandercraft gets second FDA nod for self-balancing exoskeleton
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Wandercraft gets second FDA nod for self-balancing exoskeleton

Feb. 16, 2024
By Shani Alexander
Wandercraft SAS broadened its U.S. FDA clearance for the Atalante X to include rehabilitation in individuals with spinal cord injuries at levels T5 to L5. The self-balancing exoskeleton was already given the greenlight by the FDA for use in stroke rehabilitation in December 2022. “We are thrilled to have two FDA clearances, first for stroke and now spinal cord injury, in less than a year,” CEO Matthieu Masselin, told BioWorld.
BioWorld MedTech Regulatory Orthopedics U.S. FDA

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