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CoreLink receives FDA 510 clearance for 3-D anterior lumbar interbody fusion device
10 monthes ago - By Healio
CoreLink LLC announced it received FDA 510 clearance for its Foundation 3-D anterior lumbar interbody fusion device.
“The Foundation 3-D ALIF demonstrates our increasing capabilities with 3-D printing titanium alloy,” Jay Bartling, CoreLink CEO, said in a company press release. “We're proud to have the largest ALIF cage footprint on the market, which will allow surgeons to maximize endplate contact area and hold up to 8 ccs of graft.”
Foundation 3-D uses CoreLink's propriety mimetic metal technology which reportedly
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