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Medtronic Gains FDA Approval for INFUSE with Additional PEEK Implants -

Medtronic gained FDA approval for use of Infuse™ bone graft with additional PEEK-based implants in oblique lateral and anterior lumbar interbody fusion procedures at one level. This is the second expanded indication in just over two years, following use with Clydesdale and Perimeter devices in 2015. The newly-approved indications for InfuseBone Graft are OLIF 51 procedures with Divergence-L® Interbody Fusion Device at a single level from L5-S1; OLIF 25 procedures with Pivox™ Oblique Lateral Spine System at a single level from L2-L5 and use in ALIF procedures with Divergence-L Interbody Fusion Device at a single level from L2-S1. (Medtronic plc, 4/30/18)