Surgalign Announces 100th Case Completed Utilizing its Recently Launched Cortera™ Spinal Fixation System
Surgalign received FDA 510(k) in August 2022 and Cortera and was introduced in a limited market release shortly thereafter.
- Surgalign received FDA 510(k) in August 2022 and Cortera and was introduced in a limited market release shortly thereafter.
- In a little over three months, the Company has successfully penetrated target markets and today announced the completion of the 100th case utilizing this new flagship pedicle screw system.
- The system boasts a feature-rich screw design that maintains a comparatively low profile and a newly designed locking mechanism.
- Surgalign markets products throughout the United States and in approximately 50 countries worldwide through an expanding network of top independent distributors.