The Cutting Edge of Medical Technology Content, Community & Collaboration
Time: September 1, 2015 from 10am to 1pm
Location: Online Event
Street: NetZealous LLC
City/Town: Fremont
Website or Map: http://www.compliance4all.com…
Phone: 8004479407
Event Type: webinar
Organized By: Adam Fleming
Latest Activity: Aug 5, 2015
This 3 hour Webinar is a primer and overview to the premarket notification process, i.e., a 510(k). A 510(k) is a premarket submission made to FDA to demonstrate that your device to be marketed is at least as safe and effective, that is, substantially equivalent, to a legally marketed device that is not subject to PMA.
Overview:
There are three types of Premarket Notification 510(k)s that may be submitted to FDA: Traditional, Special, and Abbreviated. The Special and Abbreviated 510(k) methods were developed under the "New 510(k) Paradigm" to help streamline the 510(k) review process.
Product modifications that could significantly affect safety and effectiveness are subject to 510(k) submission requirements under 21 CFR 807 as well as design control requirements under the Quality System (QS) regulation. Under the QS regulation, all Class II and III devices and certain Class I devices are required to be designed in conformance to 21 CFR 820.30 Design Controls. FDA provides guidance and this course will address key resources when making critical decisions.
Objectives:
Compliance4All
Adam Fleaming
Phone: +1-800-447-9407
support@compliance4all.com
www.compliance4all.com
Event Link :http://www.compliance4all.com/control/w_product/~product_id=500394LIVE/
© 2024 Created by CC-Conrad Clyburn-MedForeSight. Powered by
RSVP for Bullet Proof 510(k) – Latest FDA Changes to the Process to add comments!
Join MedTech I.Q.