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# Rebound Therapeutics Aurora Surgiscope Cleared
- URL: https://www.fdaweb.com/rebound-therapeutics-aurora-surgiscope-cleared/
- Published: 2019-01-23T12:00:00.000Z
- Updated: 2026-09-15T00:56:35.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5143204

FDA has cleared a Rebound Therapeutics 510(k) for the Aurora Surgiscope System, which the company describes as the world’s first single-use disposable neurosurgical endoscope for minimally invasive access, visualization and illumination of target neuro anatomy. The device comprises two components — a sterile, single use, neurological endoscope called the Aurora Surgiscope and a non-sterile, reusable control unit called the Image Control Box. The Image Control Box allows users to digitally control high definition video images.