Research Catalog

Title

Public health effectiveness of the FDA 510(k) clearance process : measuring postmarket performance and other select topics : workshop report / Theresa Wizemann, editor ; Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process, Board on Population Health and Public Health Practice, Institute of Medicine of the National Academies.

Publication

Washington, D.C. : National Academies Press, ©2011.

Items in the Library & Off-site

Details

Additional Authors

• Wizemann, Theresa M.
• Institute of Medicine (U.S.). Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process.

Description

xiv, 118 pages : illustrations (chiefly color); 23 cm

Summary

"The Food and Drug Administration (FDA) is responsible for ensuring that medical devices are safe and effective before they go on the market. Section 510(k) of the Federal Food, Drug, and Cosmetic Act requires a manufacturer of medical devices to notify FDA of its intent to market a medical device at least 90 days in advance. That window of time allows FDA to evaluate whether the device is substantially equivalent to a product already legally on the market (called a predicate), in which case the device does not need to go through the premarket approval (PMA) process. As part of its assessment of the FDA's premarket clearance process for medical devices, the Institute of Medicine (IOM) held a workshop on July 28, 2010 to discuss how medical devices are monitored for safety after they are available to consumers. Its primary focus was on monitoring the safety of marketed medical devices, including FDA's postmarket surveillance activities, analysis of safety concerns that resulted in medical device recalls, and non-FDA sources of adverse-event information. Public Health Effectiveness of the FDA 501(K) Clearance Process summarizes the views of the workshop participants."--Publisher's description.

Alternative Title

FDA 510(k) clearance process

Subject

• United States. Food and Drug Administration > Congresses
• United States. Food and Drug Administration
• United States. Food and Drug Administration
• Public health > Equipment and supplies > Standards > United States > Congresses
• Public health > United States > Congresses
• Public health
• Equipment Safety > standards
• Medical Device Recalls > standards
• Product Surveillance, Postmarketing > methods
• United States

Genre/Form

• Conference papers and proceedings.
• Actes de congrès.
• Congress

Bibliography (note)

• Includes bibliographical references.

Additional Formats (note)

• Also available in Open Book format via the National Academies Press home page.

Contents

Introduction -- Food and Drug Administration postmarking surveillance activities and recall studies of medical devices.

ISBN

• 9780309162067
• 0309162068

LCCN

• 2011284660
• 10.17226/13020

OCLC

• ocn747903350
• 747903350
• SCSB-9238740

Owning Institutions

Princeton University Library