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Collagen Matrix, Inc. Receives FDA 510(k) Clearance for TenoMend(TM) Collagen Tendon Wrap for the Management and Protection of Tendon Injuries
Date:5/27/2008

turn to full range of motion comparable to normal unsevered tendons. The controls in which severed tendons were repaired but not wrapped, demonstrated statistically significant reduction in range of motion. TenoMend(TM) Collagen Tendon Wrap was successful in providing a protective environment for tendon repair.

"We are committed to providing the surgical community with a full line of products to address complicated orthopaedic injuries involving hard and soft tissues. TenoMend(TM) Collagen Tendon Wrap is the first in a series of tendon repair products under development," said Shu-Tung Li, Ph.D., Founder and CEO of Collagen Matrix. "We are currently exploring potential product marketing and distribution opportunities for worldwide distribution of TenoMend(TM) Collagen Tendon Wrap, which is available immediately," he added.

Collagen Matrix, Inc. is a leader in the design and engineering of collagen- and mineral-based extracellular matrices for tissue and organ repair and regeneration. Since its inception in 1997, the Company has received many government grants for the development of collagen-based matrix products in the areas of neurological, vascular, urological, and orthopaedic tissue regeneration applications. The Company currently manufactures collagen- and mineral-based finished medical devices in the areas of neurosurgery, oral surgery, orthopedic-spine surgery, and wound care. More information about the Company can be found at http://www.collagenmatrix.com.

CONTACT:

Peggy Hansen, RAC

Sr. Director, Clinical, Regulatory,

and Quality Assurance

Tel: 201-405-1477

Fax: 201-405-1355


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SOURCE Collagen Matrix, Inc.
Copyright©2008 PR Newswire.
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