Anson Client Receives Humanitarian Device Designation
Case Study
A venture-funded development stage client was developing a technology for treatment of certain neurological disorders that presented significant market potential. In the interim, the company asked Anson Group for help in pursuing a PMA path to commercialize the technology for treatment of another, relatively low incidence disorder. Aware of the company's long term business goals, we investigated alternatives and persuaded the client to allow Anson to seek HUD designation for the device. A complicating factor was the existence of an already approved device for treating the same disorder. The approved device required irreversible surgery; our client's device did not.
After filing a request with FDA, Anson listened carefully to the Agency anticipated initial position that the existence of an approved similar device precluded HUD designation for our client's device. Over a period of a few months, Anson and the client presented evidence based on clinical experience and medical literature and regulatory precedent, and built a successful case, within the framework of the HDE regulations, that the existing device was not clinically similar. HUD designation was granted and Anson's client is proceeding on the HDE path.
Benefit to the Client
