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# Medical Device User Fee Rates Posted
- URL: https://www.fdaweb.com/medical-device-user-fee-rates-posted/
- Published: 2016-07-29T12:00:00.000Z
- Updated: 2026-09-14T21:19:36.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5136346

*Federal Register* Notice: FDA is announcing the fee rates and payment procedures for medical device user fees for fiscal year 2017\. The standard fee (adjusted base amount) for a premarket application, including a BLA, and for a premarket report and a BLA efficacy supplement, is $234,495 for FY 2017\. For a panel-track supplement, the rate is 75% of the standard fee; for a 180-day supplement —15% of the standard fee; for a real-time supplement — 7% of the standard fee; for a 510(k) premarket notification — 2% of the standard fee; for a 30-day notice — 1.6% of the standard fee; for a 513(g) request for classification information —1.35% of the standard fee; for an annual fee for periodic reporting concerning a Class 3 device — 3.5% of the standard fee. For all submissions other than a 510(k) premarket notification, a 30-day notice, and a 513(g) request for classification information, the small business fee is 25% of the standard (full) fee for the submission. For a 510(k) premarket notification submission, a 30-day notice, and a 513(g) request for classification information, the small business fee is 50% of the standard (full) fee for the submission. The annual fee for establishment registration, after adjustment, is set at $3,382 for FY 2017\. To view this notice, click [here.](https://www.gpo.gov/fdsys/pkg/FR-2016-07-29/pdf/2016-17903.pdf?ref=fdaweb.com)