Medtech company OrthoAlign has received FDA 510(k) clearance for its Lantern ASC system.
The technology is a handheld surgical navigation system designed for total joint arthroplasty procedures, including total and partial knee replacements, according to a June 3 news release from OrthoAlign.
Lantern ASC provides centers with an alternative to robotic systems that require significant investment of capital and long setup times, providing surgeons with accuracy and consistency during surgeries.
Most implant systems are compatible with Lantern ASC, the release said.
At the Becker's 23rd Annual Spine, Orthopedic and Pain Management-Driven ASC + The Future of Spine Conference, taking place June 11-13 in Chicago, spine surgeons, orthopedic leaders and ASC executives will come together to explore minimally invasive techniques, ASC growth strategies and innovations shaping the future of outpatient spine care. Apply for complimentary registration now.
