Progress Tracker Update: Tracking Abbreviated and Special 510(k)s

Abbreviated and Special 510(k) submissions can now be tracked on the FDA Progress Tracker by the Official Correspondent.

If your email program has trouble displaying this email, view as a webpage. Progress Tracker Update: Now Tracking Abbreviated and Special 510(k) Submissions Today, the U.S. Food and Drug Administration (FDA) updated the progress tracker to enable the medical device industry to track the status of Abbreviated and Special 510(k) submissions. The FDA developed both the Special and Abbreviated 510(k) Programs to facilitate the review of certain types of submissions subject to 510(k) requirements. The FDA offers online progress tracking to fulfill its Medical Device User Fee Act (MDUFA) commitments. Learn More If you are interested in updates about this feature, subscribe to email alerts. Questions about the progress tracker? If you have questions about this progress tracker, email ccp@fda.hhs.gov.

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