The knee joint is the most complex joint in the human body and is very important for exercise. External trauma or frequent excessive exercise can affect our health and even lead to muscle atrophy. On January 17, the FDA approved for the first time a personalized, home-based, wireless, app-controlled neuromuscular stimulation product, E-Vive, powered by Cymedica Orthopedics, a medical device company based in Arizona, USA. R & D, which is based on muscle activation therapy provides medical equipment and postoperative neuromuscular stimulation technology before the knee injury caused by muscle atrophy in patients with surgery, thus speeding up the recovery of the body and muscle rehabilitation.
It is understood that Cymedica Orthopedics developed this product mainly for the rehabilitation of muscles in the knee joint anterior cruciate ligament injury (ACL) and total knee replacement. The main purpose of exercise knee ligament surgery is to restore knee function and promote long-term joint health. The strength and endurance of the quadriceps are essential for normal knee function. Therefore, the normal quadriceps function is knee An important part of rehabilitation exercise after joint injury. The home-based neuromuscular stimulation system utilizes ligament repair and removal of the patient's muscle suppression. This process has a positive intervention effect and can achieve the effect of activating the quadriceps.
E-Vive, an innovative wireless technology developed and put into production by CyMedica Orthopedics, aims to solve problems related to muscle atrophy. Clinical data show that some patients who have undergone knee surgery have reduced muscle strength of the quadriceps even more than 60%, and are prone to recurrent episodes, which may lead to the possibility of re-admission treatment. Each episode will bring the patient A large sum of $4,200.
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