Centinel Spine  



Tiger Woods made his comeback with Centinel Spine.

At NASS Booth #2333, Centinel Spine will highlight its latest anterior column reconstruction technologies, as well as its recently announced partnership with one of the most winning professional athletes of all time, Tiger Woods.

Centinel Spine is the largest privately-held spine company focused on anterior column reconstruction. The company offers a continuum of trusted, brand-name motion-preserving and fusion solutions backed by over 30 years of clinical success — providing the most robust and clinically-proven Total Disc Replacement and Integrated Interbody™ portfolios in the world.

For more information prior to NASS, please visit the company’s website at www.CentinelSpine.com or contact: marketing@centinelspine.com

Brands: Centinel Spine, prodisc, STALIF, Integrated Interbody, No Profile, Ti-ACTIVE, FLX, ALTOS PCT, ACTILIF


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 Press Releases

    • As part of a long-standing partnership, Tiger Woods will detail his patient journey from debilitating back pain to his recovery and return to glory.
    • The video will include discussions with the surgical team who performed the surgery with Centinel Spine’s STALIF M-Ti™ technology.
    • Centinel Spine and Tiger Woods are working with Emmy-nominated director Kevin Foley.
    • The video was created as a joint project between Centinel Spine and Tiger Woods, working with Emmy-nominated director Kevin Foley.

    New York, NY, July 28, 2020 – Centinel Spine®, LLC, the largest privately-held spine company focused on anterior column reconstruction, today announced the release of the Tiger Woods: Reborn patient journey video.  Created in partnership with 15-Time PGA Tour Majors Winner Tiger Woods, this video is Tiger’s first-hand-account of his remarkable recovery from incapacitating back pain—directly resulting from his successful spinal fusion surgery through the support of Centinel Spine’s technology.

    Tiger Woods underwent spinal fusion surgery using Centinel Spine’s STALIF M-Ti™ Anterior Lumbar Integrated Interbody fusion device in April 2017 to alleviate ongoing, debilitating pain in his back and legs. Tiger Woods: Reborn is presented in Woods’s own words—detailing his personal challenges with spinal-related pain and reflecting upon the procedure that allowed him to regain his life and ultimately complete his PGA Tour comeback after almost three years of golf inactivity. Told through the lens of Emmy-nominated director Kevin Foley, the video also includes medical perspective from the spine surgeon who performed the procedure, as well as cinematic visuals of his comeback. The release of Tiger Woods: Reborn supports Centinel Spine’s mission to educate the public on spinal disease and treatment options that allow individuals to continue to function at a high level.

    According to Tiger Woods:

    “I wasn’t seeking a solution that allowed me to return to competitive golf, only provide relief from my pain and allow me to return to life with my family.  Playing golf again at a high level was just icing on the cake.  The Centinel Spine technology was the right solution for me and I hope sharing my story in this video will help others suffering with spine-related pain to know that solutions exist—and that there is hope.”

    “Centinel Spine is committed to advancing patient care, and an important aspect of this is furthering patient education and empowerment,” said Centinel Spine CEO Steve Murray. “The goal of our partnership with Tiger Woods is to ensure that individuals suffering from debilitating spine pain are aware that surgical solutions exist that allow individuals to continue to function at a high level. This video is an authentic account of Tiger’s patient journey and how he was able to regain his life through spine surgery, told in his own words. Hopefully, this story inspires others living with pain to seek options that may help them as well,” concluded Murray.

    Centinel Spine founded the Integrated Interbody™ category in 1988 through the launch of the revolutionary Hartshill Horseshoe product, the first anterior lumbar interbody fusion device in the world. This first-of-its-kind device was the basis for future generations of the market-leading technology platform known today as STALIF®STALIF technology has a 30-year clinical history, with over 75,000 devices implanted worldwide, and still remains the only stand-alone Integrated Interbody device demonstrating biomechanical equivalence to anterior plate and cage constructs in independent peer-reviewed publications.

    The Tiger Woods: Reborn video is available on the rediscover spine patient platform at tiger.rediscovermylife.org.

    • prodisc L is the only total disc replacement system in the U.S. approved for two-level use in the lumbar spine.
    • prodisc L has been clinically utilized across the world for over 20 years, with the first successful implantation in the U.S. in 2002.
    • Centinel Spine is the only company with FDA approved cervical and lumbar total disc replacement devices.

    New York, NY, April 14, 2020 – Centinel Spine®, LLC, the largest privately-held spine company focused on anterior column reconstruction, today announced FDA approval of two-level indications for the prodisc® L Lumbar Total Disc Replacement (TDR) system. Centinel Spine now becomes the only company in the world with an FDA-approved lumbar TDR device that has been clinically reviewed and found safe and effective for two-level use.

    The prodisc L device was first implanted in the United States during concurrent IDE studies to obtain FDA approval for one and two-level use. The first two-level implantation in the U.S. took place on January 22, 2002 by Jack Zigler, MD at the Texas Health Center for Diagnostics and Surgery, Texas Back Institute, Plano, TX as a part of the two-level study. Results from the study have been published in numerous papers and are part of the over 540 published studies on the prodisc technology platform.

    “Patients with two-level prodisc L disc replacements have done remarkably well in long-term follow-up,” Dr. Zigler noted. He continued, “We began two-level prodisc L implantations in January 2002 at the Texas Back Institute as an enrolling site in the FDA study. I have now seen multiple two-level disc replacement patients with over 15-year follow-up who are still delighted with their clinical results—and have not needed additional surgery that is commonly required after initial fusion surgery. Patients with two-level disc replacement are among my most grateful patients.”

    “The prodisc technology’s remarkable safety and efficacy profile is a tribute to the design of the device,” stated Centinel Spine CEO Steve Murray. “The longevity of the prodisc technology is due to the design principles of a stable bone interface, a consistent mechanism of action enabling guided motion, and instrumentation that facilitates efficient and reliable implantation,” Murray concluded.

    The prodisc family of devices now consists of six devices, including an anterior and anterior-lateral approach lumbar disc replacement and four cervical disc replacement implants with a variety of endplate configurations designed to enable surgeons to better suit patient anatomy. New developments to the family of products include a recently initiated clinical trial comparing the prodisc C Vivo and prodisc C SK devices with an approved TDR product as a control, in order to validate their safety and effectiveness in an FDA IDE study.


 Featured Products

  • prodisc C
    Clinically Proven Motion Preservation for the Cervical Spine....

  • No other disc replacement system has been studied more: nearly 40% of all TDR papers report on prodisc. More published lives than for any other system with over 13,000 patients reported on in over 540 articles.

    Sell Sheet: http://adr.sh/3geh/bzt3/m/m

  • prodisc L
    Clinical Proven Total Disc Replacement System for the Lumbar Spine....

    • prodisc L is the only total disc replacement system in the U.S. approved for two-level use in the lumbar spine.
    • prodisc L has been clinically utilized across the world for over 20 years, with the first successful implantation in the U.S. in 2002.
    • Centinel Spine is the only company with FDA approved cervical and lumbar total disc replacement devices.
    • Sell Sheet (http://adr.sh/3geh/bhez/m/m )
  • STALIF M
    NO PROFILE® ANTERIOR LUMBAR INTEGRATED INTERBODY™ FUSION SYSTEM...

  • Now available in 3 material options:

  • STALIF C
    NO-PROFILE® ANTERIOR CERVICAL INTEGRATED INTERBODY™ SYSTEM...

  • Now available in 3 material options:

  • STALIF L
    NO PROFILE® MIS LATERAL LUMBAR INTEGRATED INTERBODY™ SYSTEM...

  • Now available in 2 material options:


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