Medtech Insight is part of the Business Intelligence Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC’s registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 8860726.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By


Careful Scrutiny Of Leadless Pacemaker Adverse Events Urged By FDA Panel

This article was originally published in The Gray Sheet

Executive Summary

As the agency prepares for PMA submissions from Medtronic and St. Jude for first-to-market leadless pacemakers, its advisory panel emphasized the importance of large and long post-approval studies that single out individual adverse event types for measurement.


Related Content

Boston Scientific Gets Early Nod For Next Gen S-ICD


Related Companies




Ask The Analyst

Please Note: You can also Click below Link for Ask the Analyst
Ask The Analyst

Your question has been successfully sent to the email address below and we will get back as soon as possible. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts