Product Overview
Our Ventura™ system is ideal for minimally invasive transforaminal lumbar interbody approaches. This straight, bulleted implant is designed to structurally support the vertebral column oblique across the midline. Its variety of footprints can accommodate different patient anatomies and pathologies, and its simple instrumentation ensures quick and reliable implant placement.
Key Features:
• Convex surfaces for secure anatomic fit
• Bulleted insertion end for easier implantation
• Instrumentation for both open and MIS approaches
• Large graft aperture
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:
MIS PLIF/TLIF
PLIF/TLIF (https://www.seaspine.com/)
