Product Overview
The Hollywood VI system combines convex, lordotic geometry, aggressive teeth, variable insertion options, and a wide range of sizes to create a highly versatile and predictable transforaminal lumbar interbody fusion (TLIF).
Key Features
Convex, lordotic surface, for more secure anatomical fit.
Curved design allows for ease of insertion and manipulation within disc space.
Large graft window to aid in fusion.
Variable insertion options to accommodate final placement of implant.
The properties of PEEK-OPTIMA® thermoplastic are optimal for spinal implants. Its mechanical strength is close to that of cortical bone. PEEK is a biocompatible, radiolucent polymer which allows clear assessment of bony fusion.
Indications:
When used as an intervertebral body fusion device, the system is intended for spinal fusion procedures at one or two contiguous levels (L2-S1) in skeletally mature patients with degenerative disc disease (DDD). DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. DDD patients may also have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). These patients may have had a previous non-fusion spinal surgery at the involved spinal level(s). These patients should have had six months of non-operative treatment. The device is intended to be used with autograft bone graft and/or allogeneic bone graft composed of cancellous and/or corticocancellous bone and supplemental fixation.
When used as a vertebral body replacement device (VBR) the SeaSpine Spacer System is intended for use in the thoracolumbar spine (T1 to L5) to replace a collapsed, diseased, damaged or unstable complete or partial vertebral body due to tumor or trauma/fracture, to achieve anterior decompression of the spinal cord and neural tissues, and to restore the height of a collapsed vertebral body. The SeaSpine Spacer System is designed to restore the biomechanical integrity of the anterior, middle, and posterior spinal column, even in the absence of fusion for a prolonged period. Additionally, the SeaSpine Spacer System is intended for use with autograft bone graft and/or allogeneic bone graft composed of cancellous
and/or corticocancellous bone.
(QF-10-01-07-ENGL-D)
Procedures:
PLIF/TLIF (https://www.seaspine.com/)
