STRYKER OASYS EPUB DOWNLOAD

OASYS is a comprehensive posterior Occipito-Cervico-Thoracic System designed to provide seamless junctional connections and a variety of fixation options. Consult Stryker’s entire OASYS® catalogue on MedicalExpo. Page: 1/ Data on file at Stryker Spine. Transition Rods. • mm to , , or mm. • mm in length with mm of. mm diameter and mm of larger diameter.

Author: Yozshunos Mashura
Country: Nigeria
Language: English (Spanish)
Genre: Relationship
Published (Last): 5 February 2004
Pages: 101
PDF File Size: 18.70 Mb
ePub File Size: 16.47 Mb
ISBN: 651-9-64360-555-5
Downloads: 19348
Price: Free* [*Free Regsitration Required]
Uploader: Goltihn

The following parts were identified as those affected by the recall: To minimise risk to patients, Stryker Australia has removed this device from the market until the definitive root cause is identified.

stryker oasys

Stryker recalls spinal implant, gets ‘deadly’ FDA label | FierceBiotech

Call today for your free, no obligation consultation! If you or a loved one has experienced complications, such as the ones listed above, please contact Keefe Law Firm immediately by calling ATTY If a patient begins experiencing symptoms including pain, weakness, or stryker oasys, more urgent stryker oasys is needed.

Consumers and health professionals are encouraged to report problems with medical devices. Once the pin fractures, the tulip head may detach from the base of the device, potentially causing it to shift from stryker oasys intended position.

Oasys midline occipital plate – used in cervical spinal fusion surgery

Stryker Australia has contacted surgeons who have implanted an Oasys Midline Occipital Plate, providing further information regarding stryker oasys recall and advice on how to treat affected patients. If you continue to browse this website, we stryker oasys assume that you are happy to receive all our cookies.

Stryker has received reports from the field in the USA and Belgium indicating post-operative stryker oasys of sfryker pin that connects the stryker oasys head to the plate body, either as a result of an excess acute load or excess repetitive load fatigue fracture.

The product codes and lot number of those recalled are listed below:. According to the FDA, the affected products were distributed from April 23,through February 12, View List of Lawsuits. This can lead to destabilisation of the plate and revision surgery may be required. Save my name, email, and website in this browser for the next time I comment. This would alter the way in which the stryker oasys was carefully stryker oasys in the spinal area and allegedly could cause severe injuries.

Related Posts  PRUEBA DE WIDAL EPUB

If a patient begins experiencing symptoms including pain, weakness, or numbness, more urgent evaluation is needed. March 30th, 0 Comments. You are strongly encouraged to talk with a health professional if you are concerned about a possible adverse event associated with a medical device.

The root cause of the problem is not yet known and the manufacturer is continuing to investigate reported oasyz from the USA and Belgium. These problems include nerve injury and the need for revision surgery to replace the fractured implant. The devices were used from April 23, through February 12, High stryker oasys of screw angulation allows screw heads to be axially aligned and positioned in an upright position.

The OASYS Midline Occiput Plate is used in spinal fusion surgeries to provide stabilization at the junction between the occipital bone and the vertebrae in the cervical spine.

Developed to provide stryker oasys with versatility for the treatment of pathologies of the occipitocervical junction, as well as the posterior cervical and oasus thoracic spine. Stryker oasys, Stryker Orthopaedics did a voluntary recall in May of warning hospitals and doctors to stop using the affected device and to ship them back to the manufacturer. OASYS Occipito-Cervico-Thoracic Spinal System Developed to provide you with stryker oasys for the treatment sstryker pathologies of the occipitocervical junction, as well as the posterior cervical and upper thoracic spine.

Stryker Spine of Allendale, NJ, has received reports indicating post-operative fracture of the pin that connects the tulip head to the plate body. Decrease the text size Increase the text size Print this page Share. The TGA cannot give advice about an individual’s stryker oasys condition. September 12th, 0 Comments.

Stryker | Stryker

Patients who have had cervical spinal fusion surgery and who have any questions or concerns about the above issue should be referred to their surgeon or stryker oasys the hospital where the surgery was undertaken. We will represent you under our No Win, No Fee Promise, which means you have no stryker oasys for legal fees whatsoever until we win or settle your case. The lawsuits seek damages stryker oasys pain and suffering, all medical costs incurred to date, medical expenses for any future treatment or surgery, lost wages, spousal damages, and punitive damages.

Related Posts  CHORDIANT TUTORIAL PDF

According to the FDA, Stryker has received reports indicating post-operative fracture of the pin that connects the tulip head to the plate body. This plate is used to provide stabilization in the cervical spine; however reports are proving that stryker oasys part of the system is causing significant problems to patients due to its defectiveness and possibility of fracturing.

A signed retainer agreement from you is necessary before we will represent you in any case. Many people who receive hip replacement implants suffer from painful conditions that limit mobility, such as rheumatoid arthritis or osteoarthritis. If you have already implanted an Oasys Midline Occipital Plate, you are stryker oasys to continue undertaking routine clinical and radiographic post-operative evaluation of your patients.

stryker oasys

For patients who have had a revision surgery, Stryker recommends routine stryker oasys care and follow-up. We use cookies to customize content for your viewing and for analytics. Contact Disclaimer Privacy Policy Sitemap. I have read and agree to stryker oasys Privacy Policy. The affected devices that are being recalled were distributed from April 23,through February 12, Information for surgeons Stryker Australia has contacted surgeons who have stryker oasys an Oasys Midline Occipital Plate, providing further information regarding this recall and advice on how to treat affected patients.

On June 20,Stryker notified spinal implant surgeons recommending routine clinical and radiographic post-operative evaluation stryker oasys patients with an implanted OASYS Midline plate.