US FDA reduces medical device 510(k) registration fees 10% for 2017

By Stewart Eisenhart, Emergo Group The US Food and Drug Administration’s medical device registration user fees for the agency’s 2017 fiscal year have decreased nearly across the board, including 10% reductions for 510(k) premarket notifications. The 2017 user fee reductions stem from offset provisions of the Federal Food, Drug & Cosmetic Act, which came into effect after the FDA reported fee collections that exceeded appropriated cumulative amounts between the regulator’s 2013 and 2016 fiscal years. As a result, “the excess shall be credited to the appropriation account of the Food and Drug Administration and shall be subtracted from the amount of fees that would otherwise be authorized to be collected for FY 2017,” states the FDA’s notice on its 2017 user fees. Standard user fees for the 2017 fiscal year decreased for all categories except for those pertaining to Premarket Authorizations (PMA): Application Type Standard Fee 2017 Standard Fee 2016 Increase (Decrease) 510(k) $4,690 $5,228 ($538) 513(g) $3,166 $3,529 ($363) PMA, PDP, PMR, BLA $234,495 $216,388 $18,107 Panel-track Supplement $175,871 $191,041 ($15,170) 180-day Supplement $35,174 $39,208 ($4,034) Real-time Supplement $16,415 $18,297 ($1,882) BLA Efficacy Supplement $234,495 $216,388 $18,107 PMA Annual Report $8,207 $9,149 ($942) 30-day Notice $3,752 $4,182 ($430) User fees for small businesses will decrease across all categories, including for PMAs: Application Type Sma...
Source: Mass Device - Category: Medical Equipment Authors: Tags: Blog Emergo Group Source Type: news