Integra LifeSciences Launches FDA-Approved Laminoplasty System

Integra LifeSciences announced the U.S. FDA 510(k) approval and introduction of its Integra Laminoplasty System for cervical and thoracic spine.

Advertisement

The system offers various plate and screw options to treat various patient anatomies. It also has user-friendly insertion options and a retentive screw driver for a more seamless approach for surgeons.

More Articles on Devices:
X-Spine Launches Three Spine Devices in US
DePuy Synthes Spine Launches SYNFLATE Vertebral Balloon
FDA Grants 510(k) Clearance to Integra LifeSciences’ Hollywood Interbody Device

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.

Advertisement

Next Up in Spinal Tech

Advertisement

Comments are closed.