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. Other relative contraindications include obesity, certain degenerative diseases, and foreign body sensitivity. Click here to visit http: 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.

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.

EXPEDIUM Spine System – SPINEMarketGroup

The espedium 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. 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 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. Subscribe to our Newsletter.

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. The patient must be instructed in the limitations of the metallic s;ine and be warned regarding expediym bearing and body stresses on the appliance prior to firm bone healing. Pediatric pedicle screw fixation is limited to a posterior approach.

The content on this page is intended for Healthcare Professionals. Postoperative care is extremely important. The safety and effectiveness of these devices for any other conditions are unknown. Postoperative care is extremely important.

  IMM 5406 PDF

All medical devices have associated risks. 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.

Specifically, patients who because of sysyem 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.

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

Ability to build hybrid constructs for a less ysstem, muscle sparing approach. Scoliosis is a coronal plane i.

Please refer to the package insert and other labeling for a complete list of indications, contraindications, precautions and warnings. These uniquely designed system components include the: In addition, the patient’s occupation or activity level or mental capacity may be relative contraindications to this surgery.

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.

Click here to visit http: A rib hump, pelvic or shoulder height imbalance tend to common in the adolescent group. 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.

Manufactured from titanium alloy, this system provides the additional benefits of interfacing with other DePuy Synthes Shstem thoracolumbar systems such as our Cervical Posterior spine fixation system: The system consists of the following: Patients typically walk systeem a forward flexed posture being unable to stand up straight. 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.

All medical devices have associated risks.

See package insert for additional warnings, precautions and possible adverse effects. The instrument’s ease of use provides the ability to pull up or push down the spine during derotation maneuvers. If you are a patient, click here. If you are a patient, click here. 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 spinr implant failure.

  JIS G3106 PDF

Any entity or condition that totally precludes the possibility of fusion, i.

Spin Family Product Catalogue. 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. Pediatric pedicle screw fixation is limited to a posterior approach. Symptoms vary with age of onset and severity of the curvature; cosmetic problems including sitting imbalance, breathing difficulty or delayed development is common findings in infants and young children.

This product has labeling limitations. 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.

EXPEDIUM Spine System

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. See package insert for additional warnings, precautions and possible adverse effects. Please direct all other requests to one of the other DePuy Synthes Companies or career inquiries email addresses located on this page.

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.

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 systen the patient.

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

Severe osteoporosis is a relative contraindication because it may prevent adequate fixation of sline anchors and thus preclude the use of this or any other spinal instrumentation system. Please direct all other requests to one of the other DePuy Synthes Companies or career inquiries email addresses located on this systeem.