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# inTravent SoloPass Brain Imager Cleared
- URL: https://www.fdaweb.com/intravent-solopass-brain-imager-cleared/
- Published: 2021-09-14T12:00:00.000Z
- Updated: 2026-09-14T17:14:28.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5150143

FDA has cleared an inTravent Medical Partners 510(k) for the SoloPass system for aiding in the frontal placement of intra-ventricular catheters. The device is designed to provide imaging and guidance to improve the placement of external ventricular drains, according to the company.

inTravent says the device allows health professionals to visualize the ventricular system, deep within the brain, to enable precision planning and guidance. It uses 2D and 3D ultrasound imaging, artificial intelligence, and trajectory guidance for intra-procedural localization and navigation. Imaging is performed at the point of procedure, eliminating the potential for brain shift that may affect the accuracy of conventional neuro-navigation systems, it says.