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
Image courtesy of Camber Spine Technologies