Cutting Edge Spine receives FDA clearance for PEEK-enhanced cervical interbody system: 4 insights

Written by Shayna Korol | July 11, 2018 | Print  |

Cutting Edge Spine received FDA 510(k) clearance for its Evol ha-C cervical interbody system.

Here are four things to know:

1. The system is made of PEEK-Optima Ha Enhanced material supplied by Invibio Biomaterial Solutions.

2. The system is intended to improve early-onset new bone formation and bony apposition to the implant after cervical fusion procedures.

3. The Evol ha-C cervical system is Cutting Edge Spine's second Ha Enhanced PEEK-Optima system to receive FDA 510(K) clearance this year.

4. Cutting Edge Spine will release an anterior lumbar interbody fusion, a direct lateral interbody fusion and an oblique lateral interbody fusion systems later in 2018 to expand its bioactive interbody portfolio.

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