Successful FDA 510(k) submissions are critical to your market success. Incomplete or inaccurate submissions can lead to failure and may delay your product launch.
What is 510(k) FDA?
510(k) or Premarket Notification (PMN) sections of the Food, Drug and Cosmetic Act require manufacturers to notify the FDA of their intent to market a new medical device 90 days before market release. Specifically, medical device manufacturers must submit their 510(k) or PMN if they intend to introduce a device into commercial distribution for the first time or if they are reintroducing a device with significant changes that could affect its safety. Such changes can include modifications to design, material, chemical composition, energy source, manufacturing process or intended use.
What is a 510(k) submission?
Successful FDA 510(k) submissions are critical to your market success. Incomplete or inaccurate submissions can lead to failure and may delay your product launch.
Appropriately selected 510(k) testing of the predicate and submitted device must be designed and performed with the outcome documented and reported to demonstrate equivalence.
We walk you through the best approach to 510(k) submissions in our article, 5 Ways to Ensure your 510k Submission Testing Goes off Without a Hitch.
Our 510(k) testing and medical device consulting services
Element offers an extensive range of testing and consulting services to help you obtain market clearance, from chemical and mechanical testing to pharmaceutical testing for combination devices. Working closely with your regulatory team, we help you select appropriate tests for your 510(k) submission. In addition to commonly used standards, our Engaged Experts can formulate non-standard test protocols for evaluating specific functional aspects of devices for which there are no standardized tests.
For more information about our FDA 510(k) testing and medical device consulting services or to request a quote, contact us today.
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