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KinetiCor’s Motion Correction System Cleared

February 19, 2020

The FDA handed KinetiCor 510(k) clearance for its motion correction system, an addon for Siemens’ magnetic resonance imaging (MRI) scanner.

The accessory device helps track the patient’s movement in real-time using sensor-based technology, updating the patient’s current position to Siemens’ Magnetom Skyra 3T MRI scanner.

The image correction system is used for maintaining image clearness when patients move their heads during neurological MRIs, which can often lead to unclear images and the need for rescans.

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