www.fdanews.com/articles/182034-medovex-wins-ce-mark-for-denervex-system
Medovex Wins CE Mark for DenerveX System
June 5, 2017
Medovex Corp. has received a CE Mark for the DenerveX system.
The system blocks and removes capsular tissue from the facet joint in one procedure. The device’s slowly rotating burr removes targeted facet joint synovial membrane and joint surface while heat ablation destroys tissue and removes any residual nervous and synovial membrane overlying the joint.
The DenerveX System consists of the DenerveX device kit, containing a single use medical device and the DenerveX Pro-40 power generator.
The system is not yet FDA cleared. — Cynthia Jessup