Tag: interbody fusion
Life Spine announces first surgical case of ProLift Lateral HELO fixated
Life Spine has announced the first surgical case of the ProLift Lateral HELO fixated expandable lateral spacer system.
The ProLift Lateral HELO fixated with Osseo-Loc surface...
HAPPE Spine raises US$3.35 million to launch new interbody spinal fusion...
HAPPE Spine has announced the closure of a US$3.35 million Series A funding round, the proceeds of which will be used to help launch...
Lateral lumbar interbody fusion is associated with lower adjacent segment motion...
The choice of lumbar interbody fusion approach influences adjacent segment motion in a cadaveric model, according to new research published in the journal Spine,...
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...
Choosing the ideal surgical approach for improved access to the L5-S1...
Chirag A Berry (Cincinnati, USA) is an assistant professor at the University of Cincinnati College of Medicine. Here he provides a summary of his...
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...
Nexxt Spine increases Nexxt Matrixx offerings with Lordotic TLIF Oblique
Nexxt Spine has released their Lordotic TLIF Oblique interbody into the market. The product is designed for transforaminal lumbar interbody fusion (TLIF), the most...
RTI Surgical reaches 5,000 implant milestone for Fortilink interbody fusion systems...
RTI Surgical today announced a milestone of 5,000 implants of Fortilink-C, -TS and -L interbody fusion (IBF) systems with TETRAfuse 3D technology in the...
“The best of all worlds”: A surgeon’s clinical experience with the...
This advertorial has been sponsored by INVIBIO ™
Hyun W Bae, MD, is a medical director at The Spine Institute (Saint John’s Health Center, Santa...
Atlas Spine launches expandable cervical interbody fusion device
Atlas Spine has announced the successful completion of its 50th surgical procedure and over 100 devices implanted with its new HiJak AC expandable cervical...
SpineSource acquires French medical device technology
SpineSource has acquired the intellectual property assets of two spinal implant systems from Kisco International (France).
The acquisition includes the L-VARLOCK expandable lumbar cage which...
A neurosurgeon’s experience with PEEK-OPTIMA™ HA Enhanced devices
This advertorial has been sponsored by INVIBIO™
Jill Wright Donaldson, MD, is a neurosurgeon at Community Hospital North (Indianapolis, IN, USA), specialising in the surgical...
Spinal Elements announces FDA clearance of Ti-Bond titanium coating as a...
Spinal Elements has recently announced FDA clearance for claims related to the macro-, micro-, and nano-surface structure of its Ti-Bond surface coating technology. Utilising this...
Southlake Equity leads Series B round of financing to prime Titan...
Titan Spine, a medical device surface technology company focused on developing surface-enhanced spinal interbody fusion implants, has announced it has closed a substantial round...
J&J acquires 3D-printed spinal implant maker EIT
Johnson & Johnson has announced its acquisition of spinal fusion implant developer Emerging Implant Technologies for an undisclosed amount.
Norderstedt, Germany-based EIT produces 3D-printed titanium...
Spinal fusion device industry to be worth US$11 billion by 2025
A report from Transparency Market Research estimates that the total value of the spinal fusion device industry will reach US$11.0 billion (£8.2 billion, €9.3...
US FDA grants clearance to Renovis for Tesera 3D-printed interbody fusion...
Renovis Surgical Technologies has announced it has received 510(k) clearance from the US Food and Drug Administration (FDA) to market posterior lumbar Tesera porous...
Meditech Spine lumbar fusion devices receive US FDA clearance
Meditech has announced the launch of its Talos lumbar interbody fusion device comprised of PEEK hydroxyapatite (PEEK-Optima HA Enhanced, Invibio Biomaterial Solutions)—the newest generation...
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...
Stryker Tritanium PL cage displays superior bone in-growth to PEEK-only and...
A pre-clinical study of Stryker’s new 3D-printed, highly-porous Tritanium PL interbody cage has found that using the device can result in “statistically superior range-of-motion,...
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...