A recent GAO report found that while the FDA has met all medical device performance goals for the 510(k) and premarket approval (PMA) processes, review times have increased in recent years. Specifically, from FY 2005 through FY 2010, the average time to final decision for 510(k)s increased 61%, from 100 days to 161 days. Likewise, the average time to final decision for original PMAs increased from 462 days for FY 2003 to 627 days for FY 2008 (the most recent year with complete data).