SHELTON, Conn., Feb. 8, 2013 /PRNewswire/ -- 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.
(Photo: http://photos.prnewswire.com/prnh/20130208/PH56828 )
"This is an exciting and major development for the ... read more