The Company believes that the Evo Cortical Electrode is the first cortical electrode to receive FDA 510(k) clearance that uses thin film printed microcircuit technology manufactured using a fully automated photolithographic process
EDEN PRAIRIE, MN / ACCESSWIRE / December 2, 2019 / (OTCQB:NMTC), a medical device company focused on the development and commercialization of thin for recording brain activity, stimulation and ablation solutions for patients suffering from , today announced that it has received U.S. Food and Drug Administration (FDA) 510(k) clearance to market its thin film cortical electrode technology for temporary (less than 30 days) recording, monitoring, and stimulation on the surface of the brain.
The Evo Cortical Electrode product line is the result of a collaboration with both and . This thin film technology offers the potential for improved resolution during recording brain activity, future placement through a less invasive procedure, and reduced inflammation of brain tissue as demonstrated in testing conducted at the Mayo Clinic.
"This is certainly a monumental achievement for the Company," stated . "A great deal of work, perseverance and commitment from our employees, development partners, consultants and manufacturing partners made this possible. This 510(k) clearance is a critical step in executing our corporate strategy, and we look forward to working towards our goal of applying this platform to a variety of other devices for recording, monitoring and stimulation for various therapeutic applications such as epilepsy, Parkinson's Disease, spinal cord stimulation and artificial intelligence."
is a developmental stage company committed to providing minimally invasive and hi-definition solutions for EEG recording, brain stimulation and ablation solutions for patients suffering from Epilepsy, Parkinson's Disease, Essential Tremors and other related neurological disorders that may improve patient outcomes and reduce procedural costs.
Forward Looking Statement
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Investor Relations Contact:
Leah Noaeill Sr. Director of Marketing NeuroOne Medical Technologies Corporation
"Caution: Federal law restricts this device to sale by or on the order of a physician"
SOURCE: NeuroOne Medical Technologies Corporation