Cutting Edge Spine Archives - Cutting Edge Spine

Posted January 13, 2020

Cutting Edge Spine Announces FDA 510(K) Clearance of its New HA Enhanced PEEK Interbody System for a Direct Lateral Approach to the Spine, the EVOL®ha-DLIF

Cutting Edge Spine, a leader in the development and commercialization of bioactive spinal solutions, today announced the 510(K) clearance and commercial launch of the latest addition to its [...]

By bradr

In EVOL-SI

Posted August 20, 2019

FDA 510(K) Clearance of its EVOL-SI Joint Fusion System

The commercialization of the EVOL-SI system addresses the needs of orthopedic surgeons and neurosurgeons seeking superior clinical outcomes following sacral-iliac surgery. Waxhaw, NC August 20, [...]

By bradr

In EVOL®HA-C

Posted July 11, 2018

FDA 510(K) Clearance of its New HA Enhanced PEEK Interbody for the Cervical Spine, the EVOL ha-C

Cutting Edge Spine, a US leader in the development and commercialization of bio-active technologies for the spine, today announced the 510(k) clearance and commercial launch of it’s latest [...]

By bradr

In EVOS

Posted June 15, 2015

the EVOS System and FDA 510(k) Clearance

Cutting Edge Spine, a technology driven developer and marketer of highly differentiated implant systems, announced that the US Food and Drug Administration has cleared the EVOS-ha, a [...]