Mistakes in FDA Device Approval Submissions & How to Avoid Them
To launch your medical device in US, you will require FDA medical device approval. Broadly classified there are three types of FDA regulatory pathways, namely 510(k), De Novo, PMA, for FDA medical device approval. It is important to choose the correct regulatory...
FDA Breakthrough Device Designation: Criteria & Application
In this blog, we will walk you through FDA breakthrough device designation, its eligibility criteria, and application process. Additionally, we will present the benefits and challenges of the FDA’s breakthrough devices program. What is an FDA breakthrough device? An...
10 Common Reasons for US FDA Submission Denials to Avoid
The U.S. Food and Drug Administration (FDA) serves as the primary regulatory authority for medical devices in the United States. It is responsible for protecting public health. The U.S. FDA accepts several types of submissions depending on the product category, risk...