Tag: interbody fusion

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...
spinal

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 market expected to grow to US$11 billion by 2025

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...
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...

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...