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OrthAlign Reports the US FDA’s Approval of Lantern Hip Technology for Hip Arthroplasty

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OrthAlign Reports the US FDA’s Approval of Lantern Hip Technology for Hip Arthroplasty

Shots:

  • The US FDA has granted 510(k) clearance to the Lantern Hip handheld technology developed for direct anterior total hip arthroplasty with patients in the supine position
  • Lantern Hip enhances HipAlign's technology with advanced accelerometers and gyroscopes, providing surgeons real-time navigation, efficient workflow and improved accuracy in cup positioning, restoration of leg length & offset
  • The tech enables individualized cup positioning across multiple planes with live pelvic tracking & precision care without requiring pre-operative imaging or capital equipment. It is compatible with most implant systems, making it a possible choice for ASC settings

Ref: PR Newswire | Image: OrthAlign

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Disha Nankani

Disha is a content writer at PharmaShots. She is passionate and curious about recent updates and developments in MedTech and Pharma industry. She covers news related to clinical trial results and updates. She can be contacted at connect@pharmashots.com.

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