SpineSmith Receives FDA Clearance for Spinal Surgery Implant System

SpineSmith Partners, a Texas-based medical device company, has received FDA clearance for the VisuALIF interbody fusion implant system, according to a company news release.

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The VisuALIF is a two-piece, standalone device for use during intervertebral body fusion of the lumbar spine. The device is open-faced, allowing in situ graft placement, tactile feedback with a face plate attachment and device placement flush with the anterior aspect of the vertebrae.

The device is available in several product sizes and configurations designed to accommodate for a wide spectrum of patient anatomy.

Read the SpineSmith Partners news release on VisuALIF.

Read other coverage on new spine devices:

– Wenzel Spine Receives FDA Clearance on Spinal System

– ArthroCare Receives FDA Clearance for Vertebral Augmentation Device

– Orthofix Releases Spinal Deformity Correction Product

At the Becker’s 32nd Annual Meeting: The Business and Operations of ASCs, taking place October 29-31 in Chicago, ASC leaders, surgeons and healthcare executives will explore strategies to drive growth, enhance operational performance, navigate reimbursement challenges and prepare for the future of ambulatory surgery. Apply for complimentary registration now.

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