EXPEDIUM SPINE SYSTEM PDF

The EXPEDIUM Spine System incorporates technique-simplifying designs, including a state of the art internal closure mechanism and a comprehensive set of. The EXPEDIUM VERSE SPINAL SYSTEM has two configurations. The first configuration utilizes the classic solid shank, double lead threadform found on. The EXPEDIUM Spine System is a innovative spine solution with technological advancements that truly differentiate it from other systems.

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Patients typically walk in a forward flexed posture being unable to stand up straight. Subscribe to our Newsletter. The set also includes a selection of instruments that let the surgeon connect the derotation instrumentation at each vertebral level Segmental Derotationat multiple vertebral levels along the spine EnBloc Derotation or both ways.

Any entity or condition that totally precludes the possibility of fusion, i. The content on this page is intended for Healthcare Professionals.

EXPEDIUM® Spine System and EXPEDIUM® Spine System | DePuy Synthes Companies

The system consists of the following:. Scoliosis is a coronal plane i. Please direct all other requests to one of the other DePuy Splne Companies or career inquiries email addresses located on this page. If you are a patient, click here.

The surgeon must be thoroughly knowledgeable not only eexpedium the medical and surgical aspects of the implant, but must also be aware of the mechanical and metallurgical limitations of metallic surgical implants. The system consists of the following: Pediatric pedicle screw fixation is limited to a posterior approach. Postoperative care is extremely important.

This product has labeling systen. Pediatric pedicle screw fixation is limited to a posterior approach. If you are a patient, click here.

The patient must be instructed in the limitations of the metallic implant and be warned regarding weight bearing and body stresses on the appliance prior to firm bone healing. This unique system combines simplicity and versatility allowing the surgeon to design the construct based on intra-operative developments and individual patient anatomy — not the constraints of the implant system.

EXPEDIUM Spine System

Severe osteoporosis is a relative contraindication because it may prevent adequate fixation of spinal anchors and thus preclude the use of this or any other spinal instrumentation system. The safety and effectiveness of pedicle screw spinal systems have been established only for spinal conditions with significant mechanical instability or deformity requiring fusion with zpine.

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Intractable back pain, sciatica, leg weakness or numbness and gait difficulty are common reasons for surgical correction in adults. These conditions are significant mechanical instability or deformity of the thoracic, lumbar, and sacral spine secondary to severe spondylolisthesis grades 3 and 4 sipne the L5-S1 vertebra, degenerative spondylolisthesis with objective evidence of neurologic impairment, fracture, dislocation, scoliosis, kyphosis, spinal tumor, and failed previous fusion pseudarthrosis.

Other relative contraindications include obesity, certain degenerative diseases, and foreign body sensitivity. This condition can also occur along with scoliosis causing Kyphoscoliosis.

The instrument’s ease of use provides the ability to pull up or push down the spine during derotation maneuvers. Expedium Family Product Catalogue. Please refer to the package insert and other labeling for a complete list of indications, contraindications, zpine and warnings. Click here to visit http: All medical devices have associated risks.

If you would like to report a potential cybersecurity vulnerability in any of our products, please refer to our Responsible Disclosure Reporting website. The safety and effectiveness of these devices for any other conditions are unknown. Active systemic infection or infection localized to the site of the proposed implantation are contraindications to implantation. In addition, the patient’s occupation or activity level or mental capacity may be relative contraindications to this surgery.

Through unique design innovations, the EXPEDIUM Spine Spihe combines simplicity expeeium versatility allowing the surgeon to design the construct based on intra-operative developments and individual patient anatomy. Please direct all other requests to one of the other Exprdium Synthes Companies or career inquiries email addresses located on this page.

Disease conditions that have been shown to be safely and predictably managed without the use of internal fixation devices are relative contraindications to the use of these devices.

These uniquely designed system components include the: Ability to build hybrid constructs for a less invasive, muscle sparing approach. See package insert for additional warnings, precautions and possible adverse effects. Specifically, patients who because of their occupation or lifestyle, or because of conditions such as mental illness, alcoholism, or drug abuse, may place undue sjstem on the implant during bony healing and may be at higher risk for implant failure.

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The safety and effectiveness of pedicle screw spinal systems have been established only for spinal conditions with significant mechanical instability or deformity requiring fusion with expedum.

The content on this page is intended for Healthcare Professionals. A rib hump, pelvic or shoulder height imbalance tend to common in the adolescent group. The patient should be warned that noncompliance with postoperative instructions could lead to failure of the implant and possible need thereafter for additional surgery to remove the device.

This product has labeling limitations. The EXPEDIUM Spine System family of products includes a wide selection of deformity specific implants and instruments to support our philosophy of patient driven, pathology specific solutions.

Symptoms vary with age of onset and severity sywtem the curvature; cosmetic problems including sitting imbalance, breathing difficulty or delayed development is common findings in infants and young children. The implantation of pedicle screw spinal systems should be performed only by experienced spinal surgeons with specific training in the use of this pedicle screw spinal system because this is a technically demanding procedure presenting a risk of serious injury to the patient.

The implantation of pedicle screw spinal systems should be performed only by experienced spinal surgeons with specific training in the use of this pedicle screw spinal system because this is a technically demanding procedure presenting a risk spune serious injury to the patient.

The set also includes a selection of instruments that let the surgeon connect the derotation instrumentation at each vertebral level Segmental Derotationat multiple vertebral levels along the spine EnBloc Derotation or both ways.