Spineology Receives FDA Clearance for Rampart Interbody Fusion Devices

Spineology, a St. Paul, Minn.-based spine device company, has received FDA clearance for its Rampart line of interbody fusion implants, according to a Spineology news release.

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The company will now initiate a launch of the product line, which includes a variety of implant configurations to fit different patient anatomy. The implantation equipment is designed to enhance the surgeon’s ability to position the implant within the disc space.

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