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FDA APPROVES PMA FOR INTEGRA LIFESCIENCES CORPORATION'S ARTIFICIAL SKIN: FIRST OF A NEW CLASS OF TISSUE REGENERATION PRODUCTS
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PR Newswire
- Article date:
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March 4, 1996
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Copyright informationCOPYRIGHT 1996 PR Newswire Association, Inc. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan. All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)
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PLAINSBORO, N.J., March 4 /PRNewswire/ Integra LifeSciences Corporation (Nasdaq NNM: IART) announced today that it has received notification from the U.S. Food and Drug Administration (FDA) that its Premarket Approval Application (PMA) seeking permission to market the Company's INTEGRA(TM) Artificial Skin, Dermal Regeneration Template(TM) device is approved. The INTEGRA Artificial Skin product is indicated for the treatment of patients with life-threatening full-thickness or deep partial-thickness burns where conventional autograft is not available or not desirable due to the physiological condition of the patient. The Company believes that INTEGRA Artificial Skin is the ...
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