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Evonik Reaches Milestone with Permanently Implantable VESTAKEEP PEEK

Evonik noted that each of its primary implantable VESTAKEEP® PEEK product lines has been referenced in customer products that have received U.S. Food and Drug Administration's 510(k) clearance for permanent implant use.

The product lines used in medical devices that have received FDA 510(k) clearance include VESTAKEEP® i2G Resin for injection molding applications, VESTAKEEP® i4G Resin for injection molding and extrusion applications and VESTAKEEP® i4R Stock Shape for machined implant applications. (Source: Evonik Corporation)