Tag: lateral interbody fusion

Cutting Edge Spine receives FDA 510(k) clearance for EVOL ha-DLIF system

  Cutting Edge Spine has received 510(k) clearance from the US Food and Drug Administration (FDA) for its EVOL ha-DLIF direct lateral interbody fusion system. The...

Spineology completes first lateral post-market study cases using novel implant design

Spineology has announced the completion of the first post-market study cases using its recently FDA-cleared Duo Lumbar Interbody Fusion System. In October, the company...

UK’s NICE issues updated guidance on lateral interbody fusion procedures

Updated guidance has been published by the National Institute for Health and Care Excellence (NICE) in the UK for lateral interbody fusion in the...