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U.S. Department of Health and Human Services

522 Postmarket Surveillance Studies Database

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The FDA has the authority to require device manufacturers to perform postmarket surveillance under Section 522 of the Food, Drugs and Cosmetics (FD&C) Act, when questions are identified for devices that meet the statutory criteria. This database contains information about 522 Postmarket Surveillance Studies that have been required. This database allows you to search information about the postmarket surveillance requirements by manufacturer or device.

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  To search for Manufacturer beginning with a specific letter, select that letter
 
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AE and effectiveness rates


 
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General
Study Status Terminated
522 Number / Requirement Number PS120018 / PSS001
Date Original Plan Accepted 01/03/2012
Study Name AE and effectiveness rates
Device Name Supple peri-guard pericardium
Root Document Number K961810 
General Study Protocol Parameters
Study Population
Detailed Study Protocol Parameters
Study Objectives Postmarket surveillance (522) order no longer applies. Indication for Use revised and no longer include the indication subject of the 522 order.




Contact Us


Mandated Studies Program
Food and Drug Administration
10903 New Hampshire Ave.
Silver Spring, MD 20993-0002
Email: MandatedStudiesPrograms@fda.hhs.gov

Additional Resources


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