Vetera Spine Receives FDA 510(k) Clearance for Cervical Fusion Device

Atlanta, Georgia-based Vertera Spine has received FDA 510(k) clearance for its Cohere cervical interbody fusion device.

Indicated for anterior cervical discectomy fusion procedures, the device features Peek Scoria biomaterial, a proprietary porous surface technology that provides expulsion resistance.

Studies have demonstrated the advantages of adding porosity to implant surfaces to form a more stable union with bone, according to the company.

Vertera Spine is a developer of surgical solutions that use or complement its porous surface technology to address clinical needs in spine procedures. — Michael Cipriano