Tag: PLIF

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....