ADDITIONAL AUTHORIZATION OF APPROPRIATIONS FOR POSTMARKET SAFETY INFORMATION.

SEC. 215. ADDITIONAL AUTHORIZATION OF APPROPRIATIONS FOR POSTMARKET SAFETY INFORMATION. For the purpose of collecting, developing, reviewing, and evaluating postmarket safety information on medical devices, there are authorized to be appropriated to the Food and Drug Administration, in addition to the amounts authorized by other provisions of law for such purpose—(1) $7,100,000 for fiscal year 2008;(2) $7,455,000 for fiscal year 2009;(3) $7,827,750 for fiscal year 2010;(4) $8,219,138 for fiscal year 2011; and(5) $8,630,094 for fiscal year 2012.