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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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 System combines simplicity and versatility allowing the surgeon to design the construct based on intra-operative developments and individual patient anatomy. These conditions are significant mechanical instability or deformity of the thoracic, lumbar, and sacral spine secondary to severe spondylolisthesis grades 3 and 4 of the L5-S1 vertebra, degenerative spondylolisthesis with objective evidence of neurologic impairment, fracture, dislocation, scoliosis, kyphosis, spinal tumor, and failed previous fusion pseudarthrosis.

All medical devices have associated risks. 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.

This condition can also occur along with scoliosis causing Kyphoscoliosis. Manufactured from titanium alloy, this system provides the additional benefits of interfacing with other DePuy Synthes Spine thoracolumbar systems such as our Cervical Posterior spine fixation system: Click here to visit http: Any entity or condition that totally precludes the possibility of fusion, i.

If you are a patient, click here. Footer Facebook LinkedIn Twitter. Click here to visit http: The EXPEDIUM Spine System is intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of acute and chronic instabilities or deformities of the thoracic, lumbar and sacral spine.

When used for posterior non-cervical pedicle screw fixation in pediatric patients, the EXPEDIUM System is indicated as an adjunct to fusion to treat adolescent idiopathic scoliosis. Expedium Family Product Catalogue. Postoperative care is extremely important. 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.

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Pediatric pedicle screw fixation is limited to a posterior approach. Scoliosis is a coronal plane i. 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.

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Other relative contraindications include obesity, certain degenerative diseases, and foreign body sensitivity. See package insert for additional warnings, precautions and possible adverse effects. Pediatric pedicle screw fixation is limited to a posterior approach. 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.

These uniquely designed system components include the: The system consists of the following: The safety and effectiveness of pedicle screw spinal systems systrm been established only for spinal conditions with significant mechanical instability or expedlum requiring fusion with instrumentation.

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. 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.

This product has labeling limitations. All medical devices have associated risks. Intractable back pain, sciatica, leg weakness or numbness and gait expeeium are common reasons for surgical correction in adults. Specifically, patients who because of their occupation or lifestyle, or because of conditions such as mental illness, alcoholism, or drug abuse, may place undue stresses on the implant during bony healing and may be at higher risk for implant failure.

Ability to build hybrid constructs for a less invasive, muscle sparing approach. USA law restricts this device to sale sipne or on the order of physician. The surgeon must be thoroughly knowledgeable not only in the medical and surgical aspects of the implant, but must also be aware of the mechanical and metallurgical limitations of metallic surgical implants.

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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 systtem these devices for any other conditions are unknown.

EXPEDIUM Spine System

This product has labeling limitations. Please direct all other requests to one of the other DePuy Synthes Companies or career inquiries email addresses located on this page. The system consists of the following:. The instrument’s ease of use provides the ability to pull up or push down the spine during derotation maneuvers. Subscribe to our Newsletter.

See package xystem for additional warnings, precautions and possible adverse effects.

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

If you would like to report sywtem potential cybersecurity vulnerability in any of our products, please refer to our Responsible Disclosure Reporting website. Any entity or condition that totally precludes the possibility of fusion, i.

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 instrumentation. Please spjne all other requests to one of the other DePuy Synthes Companies or career inquiries email addresses located on this page. Specifically, patients who because of their occupation or lifestyle, or because of conditions such as mental illness, alcoholism, or drug abuse, may place undue stresses on the implant during bony healing and may be at higher risk for implant failure.

Active systemic infection or infection localized to the site of the proposed implantation are contraindications to implantation.

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