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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Ridhi is an avid secondary researcher who follows trends in the biopharmaceutical and healthcare sectors to curate engaging content for the global audience. She works as a news editor at PharmaShots and loves to read books and explore new destinations.
