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.
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...
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.
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