by Ariana Del Negro
Editor's Note: The following is the first in a series of articles addressing future regulatory changes for medical devices. In...
As the FDA revamps the medical device approval process, significant overhauls are expected for both the PMA and 510(k) pathways. Medtech Insight is presenting a series of articles focusing on the effect these changes will have to the industry, starting with this first installment focused on potential changes to premarket approvals.
by Ariana Del Negro
Editor's Note: The following is the first in a series of articles addressing future regulatory changes for medical devices. In...