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    Breaking News

    Spine Wave Launches Salvo 4.75 mm Spine System

    Technology will substantially strengthen the company’s position in the thoracolumbar spine fixation market.

    Related CONTENT
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    • FDA Clears Orthofix's 3D-Printed Titanium Cervical Spacer System
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    Globe Newswire10.19.20
    Spine Wave is pleased to announce the successful completion of its limited market release and the launch of the Salvo 4.75 mm Spine System, and with it, the company’s expansion into the market for thoracolumbar spinal fixation systems featuring modular screw design. The Salvo 4.75 mm Spine System will substantially strengthen Spine Wave’s position in the thoracolumbar spine fixation market and complement the company’s broad portfolio of innovative spine fusion technologies.

    The low-profile Salvo 4.75 mm Spine System is designed for both cortical bone trajectory and traditional transpedicular approaches. The small stature system features a unique modular screw design whereby the separate “tulip” and “shank” portions of the screw can be assembled in-situ after surgical decompression or on the back table prior to implantation. This versatility can enhance visibility within the surgical field even with less invasive procedures. Hospitals appreciate the system’s modular design as it provides a full complement of implant options with fewer trays to process and to keep onsite, which may reduce operating costs. The Salvo 4.75 mm Spine System is offered in titanium with the option of cobalt chromium rods that deliver the rigidity of a traditional larger 5.5 mm titanium rod.

    “Salvo is a well-designed ergonomic system that allows for ease of use by surgeons. Its low-profile stature makes it ideal for cortical bone trajectory cases,” said Ahmed M. Khan, M.D., chief of Neurosurgery at The Hospital for Central Connecticut. “And its modularity and easy to apply tulip heads make it a versatile system that is one of the best out on the market.”

    “Spine Wave is very excited to launch the Salvo 4.75 mm Spine System following a very successful limited release. The development team clearly did a superb job with this system as evidenced by the overwhelmingly positive feedback we received from the surgeons, particularly about the ease and reliability of the in-situ assembly capability,” said Mark LoGuidice, Spine Wave’s CEO. “The 4.75 mm system is just the first of many planned Salvo System modules to comprehensively address open and less invasive procedures for degenerative, deformity and revision indications.” He continued, “This is a very exciting time for Spine Wave as we recently announced our entry into the biologics market and, in addition to the Salvo System, we have plans to rapidly build out our spinal hardware portfolio in the coming quarters.”
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      Research shows using a hyaluronic acid hydrogel system temporarily stops cartilage degeneration that commonly occurs after injury.
      Sam Brusco, Associate Editor 04.09.21

    • Spine/Neurology
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      Google Executive Joins SeaSpine's Board of Directors

      Shweta Singh Maniar leads the visions, strategy and execution of Google Cloud’s industry product strategy.
      Michael Barbella, Managing Editor 04.09.21

    • HSS and LimaCorporate Open Provider-Based 3D Design and Printing Facility

      HSS and LimaCorporate Open Provider-Based 3D Design and Printing Facility

      Creates faster access to more personalized solutions to highly complex orthopedic conditions.
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    • Spine/Neurology
      Study: Spinal Fixation Rods Can Improve Patient Outcomes

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      Products allow surgeons the freedom to place rods based on patient anatomy.
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    • Orchid Welcomes New CFO

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      Matt Tharp joins the company with over 20 years of experience in supply chain, operations, and finance.
      Charles Sternberg, Assistant Editor 04.07.21

    • Spine/Neurology
      FDA Approves NuVasive

      FDA Approves NuVasive's Simplify Disc for Two-Level Cervical Total Disc Replacement

      Implant achieved the highest overall clinical success rate at both one- and two-levels compared to any other approved cervical disc.
      Michael Barbella, Managing Editor 04.07.21


    • Spine/Neurology
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      Empirical Spine's LimiFlex Device Granted Breakthrough Designation Status

      Product targets degenerative spondylolisthesis.
      Michael Barbella, Managing Editor 04.06.21

    • Spine/Neurology
      FDA Clears Orthofix

      FDA Clears Orthofix's 3D-Printed Titanium Cervical Spacer System

      Designed with nanoscale surface features, the CONSTRUX Mini Ti System is Orthofix’s first 3D-printed titanium interbody introduced to the market.
      Michael Barbella, Managing Editor 04.05.21

    • MedTorque Promotes Chad Ryshkus to VP, Commercial Operations

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      Executive will now be responsible for driving Voice of the Customer into all corners of the enterprise.
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    • Augmedics Raises $36 Million in Series C Financing

      Augmedics Raises $36 Million in Series C Financing

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    • Extremities | Spine/Neurology
      Encora

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    • Spine/Neurology
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    • MIS/Robotics
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    • MIS/Robotics | Trauma/Sports
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