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Evonik's VESTAKEEP® PEEK-based K7 LLC's Cervical Spacer Gains US FDA's 510(K) IBF Clearance

Published on 2013-02-07. Author : SpecialChem

K7 LLC's K7C™ Cervical Spacer, a spinal implant device using Evonik's VESTAKEEP® PEEK (polyetheretherketone), has received the U.S. Food and Drug Administration's (FDA) 510(k) approval for use as an Intervertebral Body Fusion (IBF) device. This marks the first time a VESTAKEEP® PEEK-based spinal fusion medical device has gained 510(k) approval from the FDA. The K7C™ Cervical Spacer is one of several PEEK-based spinal implant devices being developed by K7 LLC.

 


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