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DiFusion Technologies' Spinal Implant Made of Evonik's VESTAKEEP® PEEK Gets FDA 510(k) Approval

Published on 2013-05-27. Author : SpecialChem

Xiphos™ ALIF, a VESTAKEEP® PEEK-based (polyetheretherketone) spinal implant developed by DiFusion Technologies, has received the U.S. Food and Drug Administration's (FDA) 510(k) approval for use in Interbody Fusion Devices (IBF) devices. "DiFusion Technologies is very excited about the FDA 510(k) approval of the VESTAKEEP® PEEK-based Xiphos™ ALIF spinal implant," said Derrick Johns, managing director of DiFusion Technologies. "This milestone helps pave the way for more innovative medical devices developed from bioactive polymers.


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