FDA Clears AccelSPINE's Next Generation Minimally Invasive Spine System

Written by Anuja Vaidya | May 05, 2014 | Print  |

AccelSPINE has received U.S. Food and Drug Administration clearance on its Picasso II system.

Picasso II is intended to immobilize and stabilize spinal segments as a supplement to fusion during the treatment of acute and chronic instabilities or deformities of the spine. It is an addition to the company's Picasso product line.

 

AccelSPINE is a national medical device company that designs, develops and manufactures spinal implants and instruments.

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