OrthAlign Receives FDA 510(k) Clearance for Lantern® Hip
OrthoSpineNews
OCTOBER 3, 2024
IRVINE, Calif., Oct. 3, 2024 /PRNewswire/ — OrthAlign, Inc., a privately held medical device company, announces FDA 510(k) clearance of their Lantern Hip handheld technology for direct anterior total hip arthroplasty with the patient in the supine position. Lantern Hip is the latest addition to the Lantern platform, joining existing applications for total knee, revision knee, and partial knee … The post OrthAlign Receives FDA 510(k) Clearance for Lantern® Hip appeared first on Ortho
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