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