InTRAvent wins FDA 510(k) clearance for Solopass bedside neuro-navigation device

The inTRAvent Solopass (Photo courtesy of inTRAvent)

InTRAvent has announced FDA 510(k) clearance of its Solopass system for assisting frontal placement of intraventricular catheters deep within the brain.

The Hershey, Pennsylvania-based company said yesterday that it designed the device with 2D and 3D ultrasound imaging, artificial intelligence and trajectory guidance for intraprocedural localization and navigation for external ventricular drain (EVD) placement.

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