Camber Spine Gains FDA Clearance for Spira-C Open Matrix Cervical Interbody

By Julie A. Vetalice

Camber Spine received FDA 510(k) clearance to market the SPIRA™-C Open Matrix cervical interbody fusion device.

Like the anterior lumbar version, SPIRA-C features an arched design and is 3D-printed with Surface by Design™ technology that supports creation of a roughened titanium surface to encourage bone growth, with a pore size optimized for ingrowth. The device is intended for use with additional FDA-cleared supplemental fixation.

Source: Camber Spine Technologies, LLP

Camber Spine SPIRA-C Open Matrix Cervical Interbody Fusion Device

Image courtesy of Camber Spine Technologies

Product Labels: Spinal Fusion

Tags: 510(k) Clearance, Regulatory