Tag: titanium

Nuvasive have announced the released of the porous titanium Modulus XLIF

Nuvasive launches 3D-printed porous titanium implant Modulus XLIF

Medical device company Nuvasive have launched a new porous titanium interbody implant for their XLIF procedures, named the Modulus. The Modulus XLIF device is...
Medicrea UNID lab

World-first 360-degree personalised spine surgery takes place in UK

Patient-specific titanium instrumentation has been implanted from the front and back, creating the first ever 360-degree personalised spinal surgery. Orthopaedic surgeon Benjamin Taylor performed the...
Titan Spine Endoskeleton

Chad Kolean appointed chief financial officer of Titan Spine

Titan Spine has appointed Chad Kolean as chief financial officer. In his role, Kolean will oversee Titan’s Finance Team and work to support the...

First clinical use of Life Spine’s TiBow expandable spacer system

Life Spine has announced the first clinical uses of its TiBow minimally invasive transforaminal lumbar interbody fusion (TLIF) expandable spacer system featuring Osseo-Loc surface...
Titan Spine Endoskeleton

Titan Spine appoints Ed Graubart as vice president of Professional Development

Titan Spine has announced that Ed Graubart has joined the leadership team as vice president of Professional Development. Graubart will be responsible for enhancing...

Porous PEEK demonstrates greater osseintegration than micro-textured titanium

The virtues of polyetheretherketone (PEEK) as a material for spinal implants are well documented. PEEK’s radiolucency along with its similar strength and stiffness to...

Spinal Elements Magnum+ achieves 96% solid fusion at seven months

Data obtained from a retrospective study involving the Spinal Elements’ Magnum+ device used in anterior lumbar interbody fusion have demonstrated a 96% rate of...

Medicrea files FDA 510(k) submission for 3D-printed titanium spinal devices

Medicrea has filed a 510(k) submission to the US Food and Drug Administration (FDA) for approval of the company’s 3D-printed titanium interbody devices, with...

Surface innovation in spinal technology

Surface technology for interbody fusion implants is an area of massive growth in the spinal market, with a large number of device companies and...

SeaSpine receives two US FDA 510(k) clearances

SeaSpine has received 510(k) clearance from the US Food and Drug Administration (FDA) for its Shoreline ACS anterior cervical standalone system, featuring TruProfile technology,...

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,...

DeGen Medical introduces Latitude-C Porous Ti cervical interbody spacer

  DeGen Medical has introduced the Latitude-C Porous Ti cervical interbody spacer, an extension of the company’s Latitude-C product line. According to a company release,...

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...

K2M expands 3D-printed MIS Cascadia lateral interbody system

K2M has received 510(k) clearance from the US Food and Drug Administration (FDA) to expand its Cascadia lateral interbody system, featuring the company’s Lamellar...

Titan Spine initiates full US launch of new NanoLock surface technology

Titan Spine has expanded the distribution of its line of Endoskeleton titanium implants featuring the company’s new proprietary NanoLock surface technology to all of the...

Ulrich medical USA releases uCerv titanium cervical interbody system

Ulrich medical has announced the US market release of its uCerv titanium spinal implants as an adjunct to its current uCerv PEEK Optima interbody...

US FDA clears Life Spine’s Pro-Link Ti stand-alone cervical spacer system

Life Spine has announced that the US Food and Drug Administration (FDA) has given 510(k) marketing clearance to the company’s Pro-Link Ti stand-alone cervical...

US FDA clears Spineart Juliet Ti lumbar interbody devices

Spineart has received 510(k) clearances from the US Food and Drug Administration to market its new Juliet Ti lumbar interbody systems in the USA....

Spinal Elements reaches 10,000 Ti-Bond implant milestone, initiates warranty programme

Spinal Elements has announced that over 10,000 Ti-Bond interbody devices have been implanted. To celebrate this milestone a Ti-Bond warranty programme has been initiated. Ti-Bond...