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See today's BioWorld MedTech
Home » FDA gives green light to Mainstay Medical’s Reactiv8 device
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FDA gives green light to Mainstay Medical’s Reactiv8 device

June 22, 2020
By Meg Bryant
Mainstay Medical Holdings plc has won U.S. FDA approval for its Reactiv8 implantable neurostimulation device. The company is eyeing a commercial launch of the system in early 2021. The FDA approved Reactiv8 as an aid in managing intractable chronic low back pain associated with multifidus muscle dysfunction in adults who have failed therapy and are not candidates for spine surgery.
BioWorld MedTech Regulatory Neurology/psychiatric Nerve stimulation FDA PMA

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