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ADVISORY/Sulzer Spine-Tech Receives FDA Approval for BAK/C Cervical Interbody Fusion System.


Medical & Business Editors

ADVISORY...for Monday (April 23)

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--(BUSINESS WIRE)

Sulzer Medica medica (māˑ·dē·k  Ltd. announced that its subsidiary Sulzer Spine-Tech, based in Minneapolis, Minn., received approval from the U.S. Food and Drug Administration (FDA FDA
abbr.
Food and Drug Administration


FDA,
n.pr See Food and Drug Administration.

FDA,
n.pr the abbreviation for the Food and Drug Administration.
) to begin commercializing the BAK/C(R) Cervical cervical /cer·vi·cal/ (ser´vi-k'l)
1. pertaining to the neck.

2. pertaining to the neck or cervix of any organ or structure.


cer·vi·cal
adj.
 Interbody Fusion System.

The BAK/C device is the first cervical interbody fusion device to receive FDA approval. Approximately 150,000 cervical fusions are performed in United States United States, officially United States of America, republic (2005 est. pop. 295,734,000), 3,539,227 sq mi (9,166,598 sq km), North America. The United States is the world's third largest country in population and the fourth largest country in area.  alone with a value of $150 million. The U.S. market is assumed to grow at a rate of about 20% annually.

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Publication:Business Wire
Date:Apr 23, 2001
Words:180
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