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Checkpoint Surgical Receives FDA Breakthrough Designation for Nerve Regeneration Device

Checkpoint Surgical, Inc., a leader in hand-held, intraoperative neurostimulation technology for nerve protection and repair, announced it has received Breakthrough Device designation from the U.S. Food and Drug Administration (FDA) for the Checkpoint brief electrostimulation therapy (BEST) system. The Checkpoint BEST™ system is designed to provide electrical stimulation of peripheral nerves to promote nerve regeneration as an adjunct to surgical intervention following nerve injury, with the goal of accelerating and improving patient recovery.

“We are pleased to receive the Breakthrough Device designation from the FDA as it will allow Checkpoint Surgical to deliver this important innovation in nerve regeneration for patients much sooner,” said President and CEO Len Cosentino. “Based on the recently published research by our clinical partners Dr. Susan Mackinnon and Dr. Amy Moore at Washington University in St. Louis, we believe the Checkpoint BEST system will be transformational for the treatment of nerve injuries. We are actively enrolling patients in a clinical study of the Checkpoint BEST technology at Washington University in St. Louis and working to add additional surgeon collaborators and study sites.”

“Based on our recent animal study, I am excited to be involved in multi-center clinical trials evaluating the potential for a short period of electrical stimulation to enhance nerve regeneration and improve function,” said Dr. Susan Mackinnon, Shoenberg Professor, Plastic and Reconstructive Surgery, Chief, Division of Plastic and Reconstructive Surgery, Washington University School of Medicine.

Checkpoint Surgical is an investment in Mutual Capital Partners Fund III. Read more about the announcement here

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