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When to submit a new 510(k) for an existing device

It's understandable that changes sometimes need to be made to improve devices that are already cleared and being marketed.  Are you wondering if it's necessary to submit a new 510(k) for a device in this situation?  There are draft guidance documents issued by the FDA to help companies navigate these questions, and recent updates have been made to the recommendations.  So if you're unsure how changes affect your device status, make sure to revew the guidance documents.  See the recent press release from the FDA about this topic at http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm515174.htm

Attending 2016 NASS meeting in Boston
FDA and Additive Manufacturing for Medical Devices