MY01 Earns FDA Clearance for Continuous Compartment Pressure Monitor

May 7, 2021

MY01 has received 510(k) clearance for its Continuous Compartmental Pressure Monitor, a device that monitors patients for acute compartment syndrome (ACS), an orthopedic emergency typically caused by trauma.

The sterile, single-use device takes speedy and continuous muscle pressure measurements to identify patients experiencing ACS, in which swelling may build up and cause an increase in muscle pressure.

The pressure monitor, which comes with Bluetooth capabilities, delivers a continuous pressure microsensor directly into the patient’s muscle.

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