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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Click here to visit http: USA law restricts this device to sale by or on the order of physician. Expedium Family Product Catalogue. Pediatric pedicle screw fixation sjstem limited to a posterior approach. Postoperative care is extremely important. This product has labeling limitations. All medical devices have associated risks.

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. All inquiries can be submitted by email to: Disease conditions that have been spkne to be safely and predictably managed without the use of internal fixation devices are relative contraindications exledium 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 expefium the mechanical and metallurgical limitations of metallic surgical implants.

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

EXPEDIUM Spine System – SPINEMarketGroup

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. Other relative contraindications include obesity, certain degenerative diseases, and foreign body sensitivity.

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All medical devices have associated risks. Please refer to the package insert and other labeling for a complete list of indications, contraindications, precautions and warnings. Active systemic infection or infection localized to the site of the proposed implantation are contraindications to expedimu. 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.

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

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

Severe osteoporosis is a relative contraindication because it expesium prevent adequate fixation of spinal anchors and thus preclude the use of this or any other spinal instrumentation system.

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

EXPEDIUM Spine System

If you are a patient, click here. 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.

The content on this page is intended for Healthcare Expediu. 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.

When used for syshem non-cervical pedicle screw fixation in pediatric patients, expedum EXPEDIUM System is indicated as an adjunct to fusion to treat adolescent idiopathic scoliosis. 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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USA law restricts this device to sale by or on the order of physician. 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.

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.

Pediatric pedicle screw fixation is limited to a posterior approach. The content on this page is intended for Healthcare Professionals. Any entity or condition that totally precludes the possibility of fusion, i.

Active systemic infection or infection localized to the site of the proposed implantation are contraindications to implantation. 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 expevium impairment, fracture, dislocation, scoliosis, kyphosis, spinal tumor, and failed previous fusion pseudarthrosis.