FDA CDRH 510(k)PMA supplements for process change

“30-Day Notices and 135-Day PMA Supplements for Manufacturing Method or Process Changes, Guidance for Industry and CDRH”

This document was issued on February 19, 1998. It provides guidance on changes that are suitable for inclusion in 30- day notices and 135-day supplements. It states that any change in manufacturing needed to accomodate a change in device operating software does not qualify for a 30-day notice and reccomends that submissions for such changes be in the form of a 180 day PMA supplement or alternative submission such as a real time PMA supplement or a pilot PMA supplement.

SoftwareCPR Training Courses:

IEC 62304 and other Emerging Standards Impacting Medical Device Software

Being Agile & Yet Compliant

ISO 14971 SaMD Risk Management

Software Risk Management

Medical Device Cybersecurity

Software Verification

IEC 62366 Usability Process and Documentation

Or just email training@softwarecpr.com for more info.

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