FDA Premarket Approval Supplements and Medical Device Safety and Effectiveness
Rome, Benjamin N.
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CitationRome, Benjamin N. 2016. FDA Premarket Approval Supplements and Medical Device Safety and Effectiveness. Doctoral dissertation, Harvard Medical School.
AbstractBackground: The Food and Drug Administration (FDA) evaluates high-risk medical devices, such as cardiac implantable electronic devices (CIEDs), via the pre-market approval (PMA) process, during which manufacturers submit data demonstrating safety and effectiveness. Subsequent changes to approved high-risk devices are implemented via “supplements,” which may not require additional clinical testing.
Objective: To characterize the prevalence and characteristics of changes to CIEDs made through the PMA supplement process.
Methods: Using the FDA’s PMA database, we reviewed all CIEDs approved as original PMAs or supplements from 1979-2012. For each supplement, we collected the date approved, type of supplement (panel-track, 180-day, real-time, special, and 30-day notice), and the nature of the changes. We calculated the number of supplements approved per PMA and analyzed trends relating to different supplement regulatory categories over time. For supplements approved via the 180-day regulatory pathway, which often involve significant design changes, from 2010-2012, we identified how often additional clinical data were collected.
Results: From 1979-2012, the FDA approved 77 original and 5,829 supplement PMA applications for CIEDs, with a median of 50 supplements per original (interquartile range [IQR]: 23-87). Excluding manufacturing changes that do not alter device design, the number of supplements approved each year was stable around a mean of 2.6 supplements (standard deviation 0.9) per PMA per year. PMAs remained active via successive supplements over a median period of 15 years (IQR: 8-20), and 79% of the 77 original PMAs approved during our study period were the subject of at least one supplement in 2012. Thirty-seven percent of approved supplements involved a change to the device’s design. Among 180-day supplements approved from 2010-2012, 23% (15 out of 64) included new clinical data to support safety and effectiveness.
Conclusions: Many CIED models currently used by clinicians were approved via the PMA supplement process, not as original PMAs. Most new device models are deemed safe and effective without requiring new clinical data, reinforcing the importance of rigorous post-approval surveillance of these devices.
Citable link to this pagehttp://nrs.harvard.edu/urn-3:HUL.InstRepos:40620251