Camber Spine Commences U.S. Launch of SPIRA Open Matrix ALIF

By Julie A. Vetalice

Camber Spine Technologies received FDA 510(k) clearance and commenced U.S. launch of the SPIRA™ Open Matrix anterior lumbar interbody fusion device. SPIRA features spiral interior support arches and is built with Surface by Design™ roughened surface technology.

The spiral arches, seen below, are designed to encourage load sharing over the whole endplate as well as maximize the amount of bone graft that can be placed within the device.

This is Camber's tenth implant line on the U.S. market, and its first series built with 3D printing/additive techniques. Next launches will include SPIRA designs for the cervical, lateral and posterior lumbar spine. Leadership also mentioned the development of extremity and custom implants for salvage and complex deformity.

Source: Camber Spine Technologies, Inc.

Product Labels: Spinal Fusion

Tags: 510(k) Clearance, Regulatory