FDA provides 510(k) approval for AURORA Surgiscope for neurological surgery -Rebound Therapeutics
Rebound Therapeutics Corporation announced FDA 510k clearance of their AURORA Surgiscope System, the world�s first single-use disposable Neurosurgical Endoscope for minimally invasive access, visualization and illumination of the target neuro anatomy.
The Aurora Surgiscope System consists of two components: the sterile, single use, neurological endoscope called the Aurora Surgiscope and the non-sterile, reusable control unit called the Image Control Box. The Surgiscope has a large working channel to optimize minimally invasive surgery, and the Image Control Box allows the user to digitally control the high definition video image. Aurora Surgiscope is the world�s first single-use disposable Neurosurgical Endoscope for minimally invasive access, visualization and illumination of the target neuro anatomy.
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