Spineart’s cervical secured cage system receives FDA approval

Spineart received approval from the U.S. Food and Drug Administration for the SCARLET AC-T cervical secured cage system.

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The system is designed to combine the benefits of an interbody device and cervical plate in one implant. It aims to reducie the profile and potential risks associated with dysphagia.

 

 Spineart is a privately held medical device company focused on developing technologies in the fields of minimally invasive surgery, motion preservation, fusion, biologics and fractures treatment.

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