Tag: Spineology

Spineology launches fully endoscopic, single-tubular retractor fusion system

Spineology has announced the limited launch of OptiLIF Endo—an ultra-minimally invasive system that requires just one tubular retractor to integrate endoscopes and endoscopic equipment into...

Spineology unveils “first-of-its-kind” Duo Ti expandable interbody fusion procedure

Spineology has unveiled its Duo Ti expandable interbody fusion procedure, which combines the company’s proprietary mesh technology with porous titanium in order to deliver a...

Outcomes of SCOUT interbody fusion trial detailed

Spineology has announced that 24-month outcomes data from SCOUT clinical trial were presented by John Chi (Brigham and Women’s Hospital, Boston, USA), at the...

Spineology announces Duo Angled Instrumentation System

Spineology has announced the launch of the Duo Angled Instrumentation System. The angled instrumentation supplements the Duo Lumbar Interbody Fusion System and allows surgeons...

Spineology mesh interbody fusion technologies yield excellent/good patient satisfaction scores

Spineology has announced that two abstracts highlighting the company’s proprietary mesh technologies were presented during the 19th Annual Meeting of the International Society for...

Spineology announces new board members

Bob Paulson and Phil Soran have been appointed to Spineology’s board of directors. Phil Soran is an entrepreneur who has founded several technology companies and...

Rampart One standard ALIF interbody fusion system gains FDA clearance for...

The Rampart One Standard anterior lumbar interbody fusion (ALIF) device (Spineology) has been granted FDA clearance, allowing it to be used with or without...

Spineology completes enrollment in IDE trial for mesh fusion implant

Spineology has announced that enrollment is now complete in the company's Spineology Clinical Outcomes Trial (SCOUT) clinical trial. The SCOUT IDE, conducted under an FDA-approved...

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...

US FDA clears Spineology’s Rampart One anterior lumbar interbody fusion system

The US Food Drug Administration (FDA) has cleared Spineology’s Rampart One anterior lumbar interbody fusion system. Rampart One is designed to minimise the exposure and...
Spineology Elite

US FDA clears Spineology Elite for narrower size and expanded indication

The US Food and Drug Administration has cleared Spineology’s Elite expandable interbody fusion system for a new size and an expanded indication. Included in...

Spineology announces Palisade pedicular fixation system 100-case milestone

Spineology has announced the completion of 100 cases using its new Palisade pedicular fixation system. Palisade is one of several recent additions to Spineology’s...

Spineology announces FDA clearance of Rampart Duo interbody fusion system

The US Food and Drug Administration (FDA) has given clearance to Spineology’s Rampart Duo interbody fusion system. The Rampart Duo device is the first...

US FDA approves Spineology Rampart devices with allograft bone

Spineology has obtained US Food and Drug Administration (FDA)-clearance for the use of allograft bone with its Rampart Interbody Fusion Devices. “This approval and our...

Spineology expands relationship with US Musculoskeletal Transplant Foundation

Spineology has expanded its relationship with Musculoskeletal Transplant Foundation (MTF), the USA’s leading tissue bank. MTF will now be the sole tissue provider for...