Medtech Insight is part of Pharma Intelligence UK Limited

This site is operated by Pharma Intelligence UK Limited, a company registered in England and Wales with company number 13787459 whose registered office is 5 Howick Place, London SW1P 1WG. The Pharma Intelligence group is owned by Caerus Topco S.à r.l. and all copyright resides with the group.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By

UsernamePublicRestriction

Cyberkinetics’ Andara for spinal cord injuries

This article was originally published in The Gray Sheet

Executive Summary

Humanitarian device exemption application will be filed "later this year" by Cyberkinetics Neurotechnology Systems for use of its Andara oscillating field stimulator to promote nerve fiber regeneration and treat acute spinal cord injuries, the firm says Sept. 6. FDA has designated the system a humanitarian use device. The stimulator is intended for use within 18 days of injury to improve or restore tactile sensation and some movement in patients with quadriplegia and tetraplegia. The HDE submission will be supported by animal data and a 10-patient clinical study. Future, expanded applications may include treatment of peripheral nerve injuries, strokes and traumatic brain injuries...

You may also be interested in...



Cyberkinetics Andara OFS Spinal Nerve Repair System To Launch By Year-End

Cyberkinetics Neurotechnology Systems is gearing up to launch its Andara OFS spinal nerve repair system "as early as the fourth quarter" of this year, the firm says, pending approval of a humanitarian device exemption application announced Feb. 20

Financings In Brief

Cyberkinetics private placement to fund Andara OFS launch: Private placement raises $10 mil. to support a planned 2007 launch of the firm's Andara OFS oscillating field stimulator. The device received a humanitarian use device designation on Sept. 6, and is designed to promote nerve fiber regeneration in patients with recent spinal cord injuries, thereby improving or restoring tactile sensation and some movement in patients with quadriplegia and tetraplegia. Contingent upon FDA humanitarian device exemption (HDE) approval, a "limited" launch is expected next year (1"The Gray Sheet" Sept. 11, 2006, In Brief)...

Neurotechnology Interests Form New Trade Association To Lobby Congress

A newly formed trade association called the Neurotechnology Industry Organization (NIO) will seek greater government support for the development of therapies for brain and nervous system diseases

Latest Headlines
See All
UsernamePublicRestriction

Register

MT023968

Ask The Analyst

Ask the Analyst is free for subscribers.  Submit your question and one of our analysts will be in touch.

Your question has been successfully sent to the email address below and we will get back as soon as possible. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts

Cancel