Tag: PLIF

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,...
Life Spine receives approval from FDA

Life Spine receives FDA 510(k) clearance for ProLift micro expandable spacer...

Life Spine has received clearance from the US Food and Drug Administration (FDA) to market the ProLift micro Expandable Spacer System. ProLift micro is designed...

Camber Spine launches SPIRA-P and SPIRA-T implants for national distribution

Camber Spine has initiated the full US launch of its SPIRA-P posterior lumbar spacer and SPIRA-T oblique posterior lumbar spacer devices. News of launch comes...

Camber Spine receives FDA clearance for SPIRA-P and SPIRA-T lumbar spacer...

Camber Spine has received US Food and Drug Administration (FDA) 510(k) clearance for both its SPIRA-P posterior lumbar spacer technology and SPIRA-T oblique posterior...

icotec receives FDA clearance to market BlackArmor® Carbon/PEEK interbody cages

The latest line of icotec interbody cages, designed to optimise bony integration and post-operative visualisation, has received US Food and Drug Administration (FDA) 510(k)...

First patient enrolled in long-term Infuse posterolateral fusion study

Medtronic has announced the launch of a long-term clinical study programme to collect prospective data on rhBMP-2 (Infuse) bone graft in posterolateral fusion (PLF)...

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....