a

Spineology Receives FDA Clearance for Rampart Interbody Fusion Devices

Written by  Laura Miller | October 18, 2011
Social sharing
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.
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.

Related Articles on Spine Devices:

Spine Device Company Medicrea International Reports Revenue Growth

Spinal USA Expands, Creates Jobs

Spineology to Launch SOAR Retractor System


© Copyright ASC COMMUNICATIONS 2011. Interested in LINKING to or REPRINTING this content? View our policies here.

blog comments powered by Disqus