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    From Nitinol to Nanotubes: A Materials Science Roundtable

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    Breaking News

    FDA OKs Spinal Elements' Ti-Bond Titanium Coating as a Macro-, Micro-, and Nano-Surface

    Products featuring the surface structure have been applied in tens of thousands of procedures since introduction in 2012.

    FDA OKs Spinal Elements
    Spinal Elements' Lucent XP Expandable Lumbar Interbody System. Image courtesy of Business Wire.
    Related CONTENT
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    • Surface Tension: Surface Treatment Considerations for Orthopedics
    • FDA Initiates Device Development Challenge to Help Combat Opioid Crisis
    Business Wire11.07.18
    Spinal Elements, a Carlsbad, Calif.-based spine technology company, today announced FDA clearance for claims related to the macro-, micro-, and nano-surface structure of its Ti-Bond surface coating technology. Highlighting Spinal Elements’ portfolio are a number of products featuring Ti-Bond, including the most recently introduced Lucent XP height- and lordosis- expandable interbody device.
     
    Interbody fusion products featuring Ti-Bond technology are comprised of a PEEK body which provides the favorable modulus and imaging characteristics surgeons have come to trust while the multi-structured Ti-Bond-coated surfaces are designed to provide a favorable environment at the vertebral endplate. Since its initial introduction in 2012, products featuring the Ti-Bond surface coating technology have benefitted tens of thousands of patients.
     
    “Spinal Elements has had a long, successful experience with the clinical application of Ti-Bond technology in the spine,” stated Jason Blain, president and CEO of Spinal Elements. “This FDA clearance represents an important scientific element of the overall Ti-Bond story—one that will expand even more as the platform continues to flourish, and we provide an increasing number of technology-based solutions to improve patient outcomes.”
     
    Ti-Bond was one of the many innovations introduced to the spine fusion market by Spinal Elements. Since its introduction, other technologies have emerged, each with their own compromises when considered for fusion. Ti-Bond allows the spine surgeon to have the latest, proven technology without compromising imaging characteristics, spinal loading conditions, or long-term performance. This clearance further demonstrates the complex surface environment provided by Ti-Bond coating adjacent to boney structures.
    Related Searches
    • spinal
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    Related Breaking News

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      The new InSet Plus glenoids feature an angled articular surface.
      PR Newswire 12.10.19

    • Trauma/Sports
      OrthoGrid Systems Receives FDA 510(k) Clearance for New PhantomMSK Trauma Application

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    • Tyber Medical Opens $8M Office and Manufacturing Facility

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      Creates about 30 additional jobs for Lehigh Valley's second-fastest growing company.
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    • Extremities | Software & Quality
      FDA OKs Shoulder Surgery 3D Planner & Positioner

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      PR Newswire 12.10.19

    • Spine/Neurology
      Clinical Study of Cell Therapy for Disc Degeneration Clears Final Planned Safety Review

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    • Spine/Neurology
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    • BioPrax Biofilm Disruption Device Granted FDA Breakthrough Device Designation

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      PR Newswire 12.09.19

    • Spine/Neurology
      Orthofix Appoints New Spine Business Leader

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      Business Wire 12.05.19

    • Packaging & Sterilization
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    • Spine/Neurology
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    • 3-D Printing/Additive Mfg. | Biologics | Materials
      3D-Printed Graftless Bone Transplants Go to Clinical Trials

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      ADAM is piloting the use of ceramics and polymer in 3D-printed bone implants, able to be produced at commodity prices.
      PR Newswire 12.04.19

    • Extremities
      CrossRoads Extremity Systems Acquires Implant Systems from Surgical Frontiers

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      The add-on acquisition furthers CrossRoads' strategy to build a market-leading company in the high-growth orthopedic extremities sector.
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      Micro Spine Implant Could Restore Standing and Walking

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      RTI Surgical Appoints New Division Leaders

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    Breaking News
    • FDA OKs Shoulder Innovations' Augmented Glenoids for Total Shoulder System
    • OrthoGrid Systems Receives FDA 510(k) Clearance for New PhantomMSK Trauma Application
    • Tyber Medical Opens $8M Office and Manufacturing Facility
    • FDA OKs Shoulder Surgery 3D Planner & Positioner
    • Clinical Study of Cell Therapy for Disc Degeneration Clears Final Planned Safety Review
    View Breaking News >
    CURRENT ISSUE

    November/December 2019

    • From Nitinol to Nanotubes: A Materials Science Roundtable
    • In Good Repair: Trauma Technologies Under Review
    • Anxious Undertones: A Review of 2019
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