CROSSLINK® Plates allow spinal surgeons to convert a dual-rod construct into a frame and increase overall construct strength.
Biomechanical studies have demonstrated that CROSSLINK® Plates improve both axial and torsional stiffness, reduce motion at the bone-implant interface, and decrease the risk for fatigue breakage.
X10 CROSSLINK® Plates rigidly lock into a variety of configurations with other
Medtronic Sofamor Danek spinal systems in a manner that helps minimize anatomical interference while maximizing construct strength.
Basics and Benefits
 X10 CROSSLINK® Plates come in a multi-span and fixed design, both of which can be rigidly lock into a variety of configurations with components from other Medtronic Sofamor Danek spinal systems.
The anatomic arched design of the
X10 CROSSLINK® Plates reduces the need for contouring, improves implant fit, and avoids dural contact.
The adjustable central mechanism on the
X10 CROSSLINK® Multi-Span Plates, by functioning in a multi-axial manner, allows attachment to the rod at any orientation in the coronal, sagittal, and transverse planes.
The top-tightening locking mechanism (break-off set screws) on the X10 CROSSLINK® Plates provides true dorsal access. The break-off heads on the set screws ensure that adequate grip on the rod by the set screw has been obtained (without any need for the surgeon to guess when adequate fixation has been achieved).
In addition, the reduced volume of the X10 CROSSLINK® Plates helps minimize the complications associated with construct prominence, such as interference with anatomical features and space available for bone graft placement.
Indications
When used as a pedicle screw fixation system of the non-cervical posterior
spine in skeletally mature patients, the CD HORIZON® Spinal System is indicated
for one or more of the following: (1) degenerative spondylolisthesis
with objective evidence of neurologic impairment, (2) fracture, (3) dislocation,
(4) scoliosis,
(5) kyphosis,
(6) spinal tumor,
and/or (7) failed previous fusion (pseudarthrosis).
In addition, when used as a pedicle screw fixation system, the CD HORIZON®
Spinal System is indicated for skeletally mature patients: (a)having severe
spondylolisthesis (Gradees 3 and 4) of the fifth lumbar-first sacral (L5-S1)
vertebral joint, (b) who are receiving fusions using autogenous bone graft only,
© who are having the device fixed or attached to the lumbar
and sacral spine (L3 and below), and (d) who are having the device removed
after the development of a solid fusion mass.
When used as a posterior, non-cervical, non-pedicle screw fixation system,
the CD HORIZON® Spinal System is intended for the following indications:
(1) degenerative disc disease (as defined by back pain of discogenic origin
with degeneration of the disc confirmed by patient history and radiographic
studies), (2) spinal stenosis,
(3) spondylolisthesis, (4) spinal deformities (e.g., scoliosis, kyphosis, and
lordosis), (5) fracture,
(6) tumor resection, and/or (7) failed previous fusion (pseudarthrosis).
See package insert for labeling limitations and other important information.
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technology
It is important that you discuss the potential risks, complications, and benefits of the X10 CROSSLINK® Plates with your doctor prior to receiving treatment, and that you rely on your physician's judgment. Only your doctor can determine whether you are a suitable candidate for this treatment.
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