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.

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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.

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FDA Grants 510(k) Clearance to Integra LifeSciences’ Hollywood Interbody Device

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