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    Breaking News

    FDA OKs RTI Surgical's Dynamic Active Compression Plate

    Zero-step titanium alloy and Nitinol locking plate system provides continuous compression and torsional stability.

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    PR Newswire09.23.20
    RTI Surgical recently received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for the Dynamic Active Compression (DAC) Plate to provide stabilization and fixation of small bones of the foot. The DAC plate addresses an unmet need in the foot and ankle market and represents RTI Surgical's first 510(k) Clearance since the company became an independent player with the support of Montagu.
     
    "The DAC plate is designed to improve fusion procedures in the foot by combining the rigid stability of a plate with Nitinol's ability to provide continuous compression and ensure apposition of the bony surfaces during healing," said Dr. Constantine Demetracopoulos, Hospital for Special Surgery. The system's simplicity also provides for surgical application using minimal, straight-forward steps which address challenges of current standard plate and Nitinol staple options, without the complexity associated with more advanced options.
     
    "The DAC plate is a prime example of how we are able to leverage our core capabilities to enter a new market. Our trauma experience was crucial in creating the first hardware product we specifically designed for lower extremities in the foot and ankle space. We look forward to continuing to bring new technologies to the market to address unmet needs and help patients," said Jimmy Blanchard, Vice President of Sales. 
     
    RTI is dedicated to beginning development and design of the novel patent-pending active compression technology for other applications. As an industry-leading surgical implant supplier, RTI partners with leading medical technology companies to design and develop medical devices. RTI also designs, develops and manufactures novel technologies which are commercialized through multiple distribution channels.
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    First 3D Printed HAnano Surface Modified Implant Gets FDA Approval First 3D Printed HAnano Surface Modified Implant Gets FDA Approval
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    Safe Orthopaedics Receives FDA 510(k) Approval for Second Generation of SteriSpine PS Safe Orthopaedics Receives FDA 510(k) Approval for Second Generation of SteriSpine PS

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      DePuy Synthes Receives 510(k) FDA Clearance for VELYS Robotic-Assisted Solution

      The system is designed for use with the company's ATTUNE Total Knee System.
      PR Newswire 01.19.21

    • OrthoPediatrics Expands Agent Network in Three European Countries

      OrthoPediatrics Expands Agent Network in Three European Countries

      Broadened its reach into the largest European market of Germany, Austria, and Switzerland.
      GlobeNewswire 01.18.21

    • Spine/Neurology
      Studies Show FlareHawk Expandable Cage Delivers Favorable Fusion, Patient Outcomes

      Studies Show FlareHawk Expandable Cage Delivers Favorable Fusion, Patient Outcomes

      Data demonstrate the device’s respect for neural anatomy and conformability to bony endplates through Adaptive Geometry.
      Globe Newswire 01.18.21


    • Large Joint
      Rapid Recovery Protocol Can Lead to Increased Range of Motion After TKA

      Rapid Recovery Protocol Can Lead to Increased Range of Motion After TKA

      Study shows that an enhanced recovery program leads to optimal results after knee replacement surgery.
      American Academy of Orthopaedic Surgeons 01.15.21

    • Spine/Neurology
      Boston Scientific Releases WaveWriter Alpha Spinal Cord Stimulators in U.S.

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      Full-body MRI conditional devices combine therapy options for personalized pain relief.
      PR Newswire 01.15.21

    • New Chief Clinical Officer on Board at IncludeHealth

      New Chief Clinical Officer on Board at IncludeHealth

      New hire is a double board certified orthopedic and sports therapist.
      IncludeHealth 01.14.21


    • Imaging
      Cios Flow from Siemen Healthineers Cleared by FDA

      Cios Flow from Siemen Healthineers Cleared by FDA

      Enables easier, more efficient operation to improve patient care in the OR.
      Siemens Healthineers 01.14.21

    • CMS Expedites Breakthrough Device Access; Industry Applauds

      CMS Expedites Breakthrough Device Access; Industry Applauds

      New rule creates an accelerated Medicare coverage pathway for innovative products that the FDA deems ‘breakthrough.’
      ODT Staff 01.13.21

    • Biologics
      Surgalign Launches New Device for Bone Formation

      Surgalign Launches New Device for Bone Formation

      ViBone Moldable is the newest orthobiologics solution of Surgalign’s bone graft portfolio to support spinal fusion.
      GlobeNewswire 01.13.21


    • Orthopedic Surgical Robots Market to Exceed $4.1 Billion by 2029

      Orthopedic Surgical Robots Market to Exceed $4.1 Billion by 2029

      Surgical robots associated with advantages such as better visualization of the operating field and lessened tremor.
      Persistence Market Research 01.13.21

    • ARCH Global Precision Acquires LISI Medical Jeropa Inc.

      ARCH Global Precision Acquires LISI Medical Jeropa Inc.

      Broadens the portfolio of products and end markets served by ARCH.
      ARCH Global Precision 01.12.21

    • Large Joint
      Rice U. Computational Model Offers Help for New Hips

      Rice U. Computational Model Offers Help for New Hips

      Study incorporates fluid dynamics and more to evaluate, enhance future implants.
      Rice University 01.12.21


    • Extremities
      FDA Clears Nvision Biomedical

      FDA Clears Nvision Biomedical's Osteotomy Wedge System

      Growing product portfolio for lower extremities made of innovative bone on-growth biomaterial.
      Nvision Biomedical Technologies 01.12.21

    • Avalign Technologies Acquires Slice Manufacturing Studios

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      Adds Slice’s additive manufacturing, high tolerance subtractive manufacturing, and sterile packaging capabilities.
      Linden Capital Partners 01.11.21

    • Biologics
      Locate Bio’s CognitOss for Chronic Osteomyelitis Earns Breakthrough Status

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      Combines resorbable bone graft with bone healing properties and proprietary dual-phasic release of antibiotics.
      Business Wire 01.11.21


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    Breaking News
    • DePuy Synthes Receives 510(k) FDA Clearance for VELYS Robotic-Assisted Solution
    • OrthoPediatrics Expands Agent Network in Three European Countries
    • Studies Show FlareHawk Expandable Cage Delivers Favorable Fusion, Patient Outcomes
    • Rapid Recovery Protocol Can Lead to Increased Range of Motion After TKA
    • Boston Scientific Releases WaveWriter Alpha Spinal Cord Stimulators in U.S.
    View Breaking News >
    CURRENT ISSUE

    November/December 2020

    • Making the Grade: Orthopedic Materials Spotlight
    • Mending Mishaps: A Trauma Technology Overview
    • Life, Interrupted: The 2020 Year in Review
    • View More >

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