FDAnews
www.fdanews.com/articles/152930-fda-approves-k7c-polyetheretherketone-based-spinal-fusion-medical-device

FDA Approves K7C Polyetheretherketone-Based Spinal Fusion Medical Device

February 5, 2013
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.
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