Product Overview
Our Cambria™ cervical interbody system combines an anatomically contoured surface geometry, a wide variety of implant options and a comprehensive set of instruments to ensure construct confidence for anterior cervical interbody fusion procedures.
Key Features:
• Unique, dual-convex surface geometry
• Large graft aperture
• Biocompatible radiolucent material
• Simple instruments
Indications:
Cambria is intended to be used as an adjunct to spinal fusion procedures at one or two contiguous levels (C3â€C7) in skeletally mature patients with degenerative disc disease (defined as neck pain with discogenic origin with degeneration of the disc confirmed by history and radiographic studies) of the cervical spine. Patients should have received at least six weeks of nonâ€operative treatment prior to treatment with the device. Devices are intended to be implanted via an open, anterior approach and used with autograft bone graft and/or allogeneic bone graft composed of cancellous and/or corticocancellous bone and supplemental fixation, such as an anterior plating system.
(QF-10-01-22-ENGL-C)
Procedures:
ACDF (https://www.seaspine.com/)
