Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Monday, December 5, 2022

FDA grants clearance for neurological monitoring device

 Our stroke leadership and researchers should immediately see this as a way to see and decode the signals that occur during neuroplasticity; seeing what is being done to a neuron to drop its' current task and take on a neighboring task. But is it better than these other methods? 

 

FDA grants clearance for neurological monitoring device

Medical device company WISE Srl announced the FDA granted clearance for its Cortical Strip, a single-use device intended to be used on the brain surface for intraoperative neurophysiological monitoring.

According to the company’s release, the novel device is the first to receive FDA clearance within the product family and follows the European CE mark already received by the product in May 2021.

Operating room during surgery
Medical device company Wise Srl announced it was given FDA clearance for its cortical strip device to be used for monitoring during brain surgery. Source: Adobe Stock

The WISE Cortical Strip is intended for intraoperative use with recording, monitoring and stimulation equipment for the recording, monitoring, and stimulation of electrical signals on the brain surface, per the release. Unlike traditional cortical electrodes, which are made of stiff metal discs enclosed in a thick silicone foil, the WISE Cortical Strip is composed of stretchable platinum contacts embedded in a soft and thin film of silicone. As a result, the WISE Cortical Strip is highly ergonomic and conformable to the brain surface, the company stated.

“FDA clearance is a crucial milestone for our commercial development, allowing [us] to expand the distribution of the WISE Cortical Strip from Europe to the US and fueling the development of the WISEneuro Monitoring product family,” Luca Ravagnan, CEO of WISE stated in the release. “European clinicians are already demonstrating strong appreciation for the benefits of our product; we are looking forward to starting commercialization also in the U.S.”

Performance of the cortical strip has been successfully validated in a multicentric premarket clinical study in Europe, the WIN study, which demonstrated safety and usability of the product. The company further revealed in the release that a study featured in Clinical Neurophysiology showed that the WISE Cortical Strip performed better in terms of electrical impedance in physiological conditions than conventional cortical electrodes available on the market; the strip also demonstrated better adhesion, conformability and stability on the brain surface.

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