Life Spine Gains FDA Clearance for Hinged Laminoplasty System

By Julie A. Vetalice

Life Spine received FDA 510(k) clearance to market a Hinged Laminoplasty System, featuring a novel retaining screwdriver and intuitive instrumentation. The hinge supports a custom fit and reduces intraoperative plate bending. This represents Life Spine’s fifth 510(k) in 2019 and their 86th overall.

Hinged Laminoplasty joins the company's lineup of Posterior Cervical solutions including the SOLSTICE® Occiptio-Cervico-Thoracic System of hooks, prebent rods, transition components, cross connectors and a Cranial Fusion Plate.

Source: Life Spine

Tags: 510(k) Clearance, Regulatory