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Gyder Surgical Reports the US FDA’s 510(k) Clearance for Gyder Hip System

Shots:

  • The US FDA has granted 510(k) clearance to the Gyder Hip System for positioning of the acetabular cup during anterior hip arthroplasty following approval from Australia’s TGA
    Gyder Hip System eliminates the use of metallic pins & pre-operative/intra-operative imaging for landmark registration, offering a less invasive approach than conventional hip navigation
  • System features 1min calibration & quick registration, providing a rapid, easy-to-use, computer-assisted navigation solution for ambulatory surgery centers (OPD) & existing surgical workflows with successful cases performed in Australia & India

Ref: Globenewswire | Image: Gyder Surgical

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