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

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. All medical devices have associated risks.

EXPEDIUM Spine System

If you would like to report a potential cybersecurity vulnerability in any expecium our products, please refer to our Responsible Disclosure Reporting website. The patient must be instructed systsm the limitations of the metallic implant and be warned regarding weight bearing and body stresses on the appliance prior to firm bone healing. Postoperative care is extremely important. Pediatric pedicle screw fixation is limited to a posterior approach.

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Intractable back pain, sciatica, leg weakness or numbness and gait difficulty are common reasons for surgical correction in adults.

Severe osteoporosis expdeium 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 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.

EXPEDIUM Spine System – SPINEMarketGroup

Patients typically walk in a forward flexed posture being unable to stand up straight. The safety and effectiveness of these devices for any other conditions are unknown.

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: 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.

USA law restricts this device to sale by or on the order of physician. 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.

Scoliosis is a coronal plane i.

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If you are a patient, click here. Expedium Family Product Catalogue.

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. 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. A rib hump, pelvic or shoulder height imbalance tend to common in the adolescent group.

All medical devices have associated risks. 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 apine fusion pseudarthrosis.

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

This product has labeling limitations. If you are a patient, click here. The content on this page is intended for Healthcare Professionals.

The instrument’s ease of use provides the ability to pull expedkum or push down the spine during derotation maneuvers. 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. 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.