K2M Expands Complex Spine Product Offering with 510(k) Clearance for SANTORINI Corpectomy Cage Systems
Summary
Leesburg, VA, March 03, 2012 --( SANTORINI cages, manufactured from biocompatible PEEK polymer, allow for an unobstructed view of the post-operative fusion and will be available as both solid and expandable options in a variety of sizes.The company is recognized as a worldwide leader in providing unique technologies for the treatment of deformity, degenerative, trauma, and tumor spinal patients.Media Contact Zeno Group on behalf of K2M, Inc. Marcie Kohenak, 202-965-7811 Marcie.Kohenak@ZenoGroup.com Leesburg, VA, March 03, 2012 --( PR.com )-- K2M, Inc., a spinal device company developing innovative solutions for the treatment of complex spinal pathologies and minimally invasive procedures, today announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market the SANTORINI™ Corpectomy Cage Systems.This new addition to the company’s growing complex spine portfolio is designed to replace collapsed, damaged, or unstable vertebral bodies due to trauma or tumor and provide anterior spinal column support.SANTORINI cages, manufactured from biocompatible PEEK polymer, allow for an unobstructed view of the post-operative fusion and will be available as both solid and expandable options in a variety of sizes.The company is recognized as a worldwide leader in providing unique technologies for the treatment of deformity, degenerative, trauma, and tumor spinal patients.