Dymicron®, a privately held medical device company pioneering advanced spinal technologies, today announced that the United States (U.S.) Food and Drug Administration (FDA) has granted Investigational Device Exemption (IDE) approval to begin a pivotal clinical study of the Triadyme®‑C cervical artificial disc. This achievement marks a critical milestone in the company’s mission to bring the next-generation cervical artificial disc to patients suffering from degenerative disc disease.
10
Jul
Dymicron Granted IDE Approval for Triadyme-C Artificial Disc
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