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Home » FDA Clears Standalone Cervical Interbody Fusion Device
FDA Clears Standalone Cervical Interbody Fusion Device
![ClearanceStamp_Blue.gif](https://www.fdanews.com/ext/resources/test/Device_Images6/ClearanceStamp_Blue.gif?t=1576043968&width=430)
The FDA granted 510(k) clearance to Atlas Spine’s standalone version of its expandable cervical interbody system, HiJAK SA.
The adjustable implant features textured titanium-alloy endplates for better osseointegration. The implant’s curvature can be adjusted by up to 20 degrees.
The company said it plans to launch the product this summer.
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