Product Overview
Our user-friendly Redondo™-L lateral lumbar interbody spacer is designed in a variety of lengths, widths and heights to accommodate varying pathologies and patient anatomies. The anatomic, bullet-nosed interbodies have a large central aperture for autogenous bone graft to enable maximum fusion potential. A comprehensive set of exposure and disc preparation instruments complements the Redondo-L system and enables a streamlined approach to minimally invasive lateral procedures.
Key Features:
• Multiple footprints and lordotic options
• Large graft aperture
• Simple instruments
Indications:
When used as an intervertebral body fusion device, Redonodo-L 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 autogenous bone graft and supplemental fixation.
When used as a vertebral body replacement device (VBR) Redondo-L 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. Redondo-L 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, Redondo-L is intended for use with bone graft.
(QF-10-01-32-ENGL-C)
Procedures:
LLIF (https://www.seaspine.com/)