Centinel Spine Receives FDA Clearance for ALIF System

Centinel Spine received FDA clearance for the STALIF MIDLINE system for anterior lumbar interbody fusion, according to a company news release.

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The STALIF MIDLINE system includes the Lag Effect Fixation and Lumen Locking as well as ABO screw technology which guard against screw back-out. The system includes the full spectrum of implant sizes to accommodate for individual patients.

Read the Centinel Spine release on STALIF MIDLINE.

Read other coverage on spinal devices:

– Wenzel Spine Receives FDA Clearance on Spinal System

– ArthroCare Receives FDA Clearance for Vertebral Augmentation Device

– Aesculap Launches New Pedicle Screw System

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