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Home » FDA Grants Clearance for Device Using Spinal Elements’ Titanium Coating
FDA Grants Clearance for Device Using Spinal Elements’ Titanium Coating
![ClearanceStamp_Blue.gif](https://www.fdanews.com/ext/resources/test/Device_Images6/ClearanceStamp_Blue.gif?t=1576043968&width=430)
November 8, 2018
Carlsbad, California spinal tech company Spinal Elements announced that the FDA granted clearance for its expandable interbody device using its Ti-Bond surface coating technology.
The device, the Lucent XP height and lordosis expandable interbody device, uses the company’s Ti-Bond titanium porous coating technology.
The coating gives increased surface topography and immediate stability for expandable interbodies. It is hydrophilic and radiolucent.
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