The U.S. Food and Drug Administration today approved the first spinal tether device intended to be used in children and adolescents to correct the most common form of scoliosis, called idiopathic ...
The FDA approved the first spinal tether medical device to correct the most common form of scoliosis in children and adolescents—a ropelike implant that pulls the vertebrae into shape as the child ...
The US Food and Drug Administration (FDA) has approved the first spinal tether device to correct idiopathic scoliosis in children and adolescents who fail to respond to conservative treatment options, ...
The Food and Drug Administration (FDA) has approved a unique device for pediatric patients with idiopathic scoliosis who have not responded to conservative treatment options. The Tether Vertebral Body ...
Please provide your email address to receive an email when new articles are posted on . Auctus Surgical recently received FDA breakthrough device designation for its vertebral body tethering system ...
Please provide your email address to receive an email when new articles are posted on . Zimmer Biomet Holdings Inc. announced it has received FDA approval for The Tether, the first spinal tether ...
Mount Sinai surgeons have performed the first-ever spinal tethering surgery in New York City to correct idiopathic scoliosis - a sideways curvature in the spine - in children and adolescents. The ...
Scoliosis is the most common spinal deformity affecting pediatric patients. A posterior spinal fusion (PSF) is the gold standard treatment for patients with curves exceeding 45 degrees, but the ...
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