DEPUY SPINE EXPEDIUM PDF

EXPEDIUM VERSE Spinal System enables surgeons to perform multiple correction maneuvers with one versatile implant. FIGURE 1. 1. DePuy Synthes. eXpedIum spine system is a comprehensive thoracolumbar spinal system that offers DePuy Spine EMEA is a trading division of DePuy International Limited . The EXPEDIUM Spine System is a rod based platform. benefits of interfacing with other DePuy Synthes Spine thoracolumbar systems such.

Author: Tygodal Gojas
Country: Reunion
Language: English (Spanish)
Genre: Love
Published (Last): 13 April 2013
Pages: 206
PDF File Size: 14.39 Mb
ePub File Size: 2.6 Mb
ISBN: 258-5-51263-243-1
Downloads: 48981
Price: Free* [*Free Regsitration Required]
Uploader: Zululkis

USA law restricts depuu device to sale by or on the order of physician. See package insert for additional warnings, precautions and possible adverse effects.

A drag mechanism enables the implant head to retain alignment, simplifying rod capture. Please direct all other requests to one of the other DePuy Synthes Companies or career inquiries email addresses located on this page. Footer Facebook LinkedIn Twitter. Pediatric pedicle screw fixation is limited to a posterior approach. Pediatric pedicle screw fixation is limited to a posterior approach.

EXPEDIUM Spine System

Active systemic infection or infection localized to the site of the proposed implantation are contraindications to implantation. The content on this page is intended for Expediim Professionals. All medical devices have associated risks.

All inquiries can be submitted by email to: 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 instrument’s ease of use provides the ability to pull up or push down the spine during derotation maneuvers.

Other relative contraindications include obesity, certain degenerative diseases, and foreign body sensitivity. Please direct all other requests to one of the other DePuy Synthes Companies or career inquiries email addresses located on this page. The content on this page is intended for Healthcare Professionals.

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 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 experium procedure presenting a risk of serious injury to expsdium patient.

  CONTINUOUS DELIVERY JEZ HUMBLE PDF

Intractable back pain, sciatica, leg weakness or numbness and gait difficulty are common reasons for surgical correction in adults. The safety and effectiveness of these devices for any other conditions are unknown.

See package insert for additional warnings, precautions and possible adverse effects. If you would like to report a potential cybersecurity vulnerability in any of our products, please refer to our Responsible Disclosure Reporting website.

EXPEDIUM Spine System – SPINEMarketGroup

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

Please refer to the package insert and other labeling for a complete list of indications, contraindications, precautions and warnings. The surgeon must be thoroughly knowledgeable not only in deput medical and surgical aspects of the implant, but must also be aware of the mechanical and expedikm limitations of metallic surgical implants.

All inquiries can be submitted by email to: 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.

Subscribe to our Newsletter.

The safety and effectiveness of these devices for any other conditions are unknown. 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 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.

Click here to visit http: If you would like to report a potential cybersecurity vulnerability in any of our products, please refer to our Responsible Disclosure Reporting website. 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.

Patients typically walk in a forward flexed posture being unable to stand up straight. The content on this page is intended for Healthcare Professionals. Pediatric pedicle screw fixation is limited to a posterior approach. 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.

  DEATH AND THE MAIDEN ARIEL DORFMAN PDF

Please direct all other requests to one of the other DePuy Synthes Companies or career inquiries email addresses located on this page. This product has labeling limitations.

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

If you are a patient, click here. All medical devices have associated risks.

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. Please refer to the package insert and other labeling for a complete list of indications, contraindications, precautions and warnings. The system consists of the following:. 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 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. 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.

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 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.

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.