www.fdanews.com/articles/190074-rebound-therapeutics-grabs-fda-clearance-for-surgiscope-system
Rebound Therapeutics Grabs FDA Clearance for Surgiscope System
February 1, 2019
Rebound Therapeutics has received 510(k) clearance for its Aurora surgiscope system for minimally invasive neurosurgery.
The disposable, minimally invasive device enables physicians to illuminate and visualize a patient’s neuro anatomy and works with operating room high definition flat panel displays.
The device consists of two parts: the sterile, single use neurological endoscope and a non-sterile, reusable control unit that allows the user to control the high-definition video image produced.