CARLSBAD, Calif., Nov. 19, 2007 (PRIME NEWSWIRE) -- Alphatec Holdings, Inc. (NasdaqGM:ATEC - News), a medical technology company focused on the design, development, manufacturing and marketing of products for the surgical treatment of spine disorders, announced today that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market its ZODIAC LUXE(tm) 4.0mm diameter pedicle screw in concert with ZODIAC(tm) spinal disorder solution products.
