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    Life Spine Announces Initial Cases and Multiple Surgeries for PROLIFT® Expandable Interbody System

    Investing News Network
    May. 12, 2016 09:04AM PST
    Medical Device Investing

    HUNTLEY, Ill.–(BUSINESS WIRE)–Life Spine, a medical device company that designs, develops, manufactures and markets products for the surgical treatment of spinal disorders, announced today that the company has successfully completed initial cases with the PROLIFT Expandable Interbody System, which restores disc height, in-situ, for minimally invasive PLIF, TLIF and oblique approaches. The U.S. Food and …

    HUNTLEY, Ill.–(BUSINESS WIRE)–Life Spine, a medical device company that designs, develops,
    manufactures and markets products for the surgical treatment of spinal
    disorders, announced today that the company has successfully completed
    initial cases with the PROLIFT Expandable Interbody System, which
    restores disc height, in-situ, for minimally invasive PLIF, TLIF and
    oblique approaches. The U.S. Food and Drug Administration (FDA) provided
    510(k) marketing clearance to the PROLIFT System in March 2016.
    “The biggest challenge in performing interbody fusions is to place a
    large enough spacer without excessive traction along the nerves. The
    ProLift device allows for standard protection of the neurological
    structures and little to no actual traction applied to the nerves,” said
    Alexander Bailey, MD, of Precision Spine & Orthopaedic Specialists in
    Kansas City, Kansas. “As an added benefit of this design, the in-situ
    distraction achieved after placement in the desired location creates a
    situation in which migration or expulsion is nearly eliminated. I found
    the design intuitive and easy to use. Additionally, it saves procedural
    time by not requiring segmental compression, is safer due to small
    initial insertion size, and meets my needs for this type of challenging
    surgery.”
    “During my initial procedures, bilateral grafts were delivered through
    two-inch incision sites which allowed for minimal muscle disruption;
    allowing my patients to go home post-op day one. Distraction
    capabilities were easily maximized, and used in conjunction with
    CENTERLINE™ Midline Screws, I was able to create a minimally
    invasive yet robust final construct,” said John Anson, MD, FACS, of the
    Spine and Brain Institute of Las Vegas, Nevada.
    PROLIFT is scheduled for limited release in the second quarter of 2016,
    with full product release expected later in the year.
    About Life Spine
    Life Spine is dedicated to improving the quality of life for spinal
    patients by increasing procedural efficiency and efficacy through
    innovative design, uncompromising quality standards, and the most
    technologically advanced manufacturing platforms. Life Spine, which is
    privately held, is based in Huntley, Illinois. For more information,
    please visit: https://www.lifespine.com.
    Life Spine is a registered trademark.

    medical device companyfood and drug administration
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