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      Stryker Unveils Hoffmann LRF Hexapod With Pre And Post-Operative Planning Tool For Deformity Correction & Limb Reconstruction Procedures

      Advanced Hardware Designed to Enhance Consumer Experience, While New Online Application Calculates Measurements from X-Ray Upload, Creating a Patient-Specific Plan for Surgeons

      Stryker

      News provided by

      Stryker Orthopaedics

      Jun 29, 2017, 09:00 ET

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      MAHWAH, N.J., June 29, 2017 /PRNewswire/ -- Stryker's Foot and Ankle business unit today announced the upcoming launch of its new Hoffmann LRF Hexapod hardware and online application, featuring an advanced measurement tool that uses a mathematical algorithm to calculate solutions to correct the deformity. Hoffmann LRF Hexapod is being demonstrated during the American Orthopaedic Foot & Ankle Society (AOFAS) annual meeting from July 12-14 in Seattle.

      "Stryker's Hoffmann LRF Hexapod and its innovative software is a step forward for surgeons and patients involved with complex deformity correction and limb reconstruction procedures. The product is the first-of-its-kind, offering top, as opposed to side, actuating struts, making it easier for patients to reach and manage the hardware," said John Sontich, MD, Chief of Orthopaedic Trauma at University Hospitals Cleveland Medical Center and past president of the Limb Lengthening and Reconstruction Society. "I am looking forward to using these new technologies to help enhance the patient experience from the first consultation to the end of someone's treatment."

      Unlike traditional pre-planning, surgeons can upload a patient's x-rays into the software, which then calculates a treatment solution based on manual inputs by the surgeon, creating a patient-specific plan for strut adjustments. The Hoffmann LRF Hexapod hardware features the core components of Hoffmann LRF with additional flexibility of strut offsetting, allowing the user to relocate the struts to a more optimal position.

      Based on the simplicity and reliability of the original Hoffmann Fixator, the versatile Hoffmann LRF product line is designed to match today's biological repair and reconstruction methods.

      "Our team is excited to showcase the benefits of the Hoffmann LRF platform and its intuitive software at AOFAS," said Tom Popeck, Vice President and General Manager of Stryker's Foot and Ankle business unit. "We believe this modern deformity correction platform helps streamline the surgical planning process and demonstrates our dedication to moving technology forward with our surgeons and patients best interest in mind."

      Other products and services that will be showcased at Stryker's AOFAS exhibit (booth #1001) include:

      • VariAx 2® Fracture Plates
        VariAx 2® Fracture Plates are SOMA designed for an enhanced fit. These plates are available in a variety of lengths and sizes (two to seven holes), offered in slim and broad options, and indicated for the foot, ankle, hand and wrist.

      • ToeTac
        ToeTac is a sterile-packed PEEK cannulated hammertoe fixation product that does not require cold chain storage and includes cup and cone reamers allowing for simple K-wire fixation of adjacent joints.

      • M.O.R.E. (Mobile Operating Room Experience)
        M.O.R.E. is designed to educate the entire surgical care team on Stryker's products and surgical techniques, providing a hands-on experience in their local community.

      For more information about Hoffmann LRF product line, please visit https://footankle.stryker.com/en/products. Surgeons may request or access their account by visiting https://fixmyleg.stryker.com.

      About Stryker
      Stryker is one of the world's leading medical technology companies and, together with our customers, we are driven to make healthcare better. The Company offers a diverse array of innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes. Stryker is active in over 100 countries around the world.

      This document is only approved for use in the USA.
      Content ID: H-BL-10, 06-2017

      SOURCE Stryker Orthopaedics

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