Decoding 21 CFR Part 814: A Guide to the FDA's Premarket Approval Pathway

Medical Device Global Market Access · Aug 11, 2025 · 3m

This episode provides a detailed overview of the FDA's Premarket Approval (PMA) process, governed by 21 CFR Part 814. We explore the requirements for Class III medical devices, the necessary components of a PMA submission, including non-clinical and clinical data, the FDA's review timeline and procedures, and the post-approval responsibilities of manufacturers. • What is a Premarket Approval (PMA) and which devices require it? • How does the FDA define a Class III medical device? • What are the essential components of a PMA application under 21 CFR Part 814? • What kind of data is required in…