ChoiceSpine received 510(k) clearance from the U.S. Food and Drug Administration for the THUNDERBOLT Minimally Invasive Pedicle Screw System.
The system is designed for a small incision procedure with streamlined instrumentation. "The THUNDERBOLT Minimally Invasive Pedicle Screw System is the fourth 510K ChoiceSpine has received in 2014 and we are looking forward to launching five more new systems in the next 12 months. We are really excited about what THUNDERBOLT brings to our product portfolio as it gives us a sleek and easy-to-use minimally invasive pedicle screw system. THUNDERBOLT will give us an offering that we have never had before," said Anderson Collins, director of business development at ChoiceSpine.
ChoiceSpine focuses on providing high-quality products to orthopedic physicians and neurosurgeons. In June, it received U.S. Food and Drug Administration 510(k) clearance for its BLACKBIRD Posterior Cervical Spinal System.
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