f Post-Approval Studies (PAS) Database
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U.S. Department of Health and Human Services

Post-Approval Studies (PAS) Database
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The FDA has the authority to require sponsors to perform a post-approval study (or studies) at the time of approval of a premarket approval (PMA), humanitarian device exemption (HDE), or product development protocol (PDP) application. Post-approval studies can provide patients, health care professionals, the device industry, the FDA and other stakeholders information on the continued safety and effectiveness (or continued probable benefit, in the case of an HDE) of approved medical devices. This database allows you to search Post-Approval Study information by applicant or device information.

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Sort By Application Number Application
Number		 Sort By Application Number -- Descending
Sort By Manufacturer Applicant Sort By Manufacturer -- Descending
   Sort By Device Name Device
Name		 Sort By Device Name -- Descending
Sort By Medical Specialty Medical
Specialty		 Sort By Medical Specialty -- Descending
Sort By Date Order Date PMA
Approved		 Sort By Date Order -- Descending
Study
Name
Study Status
P040023 DEPUY ORTHOPAEDICS, INC. DURALOC OPTION CERAMIC HIP SYSTEM Orthopedic 05/03/2005 Duraloc Long Term Redesigned/Replaced Study
Prospective Post-Approval Study Terminated
DePuy Outcome Tracking Sys Registry(DOTS) Terminated
Kaiser Permanente Joint Registry Terminated
Natl Joint Registry for England and Wales Terminated
Australian Ortho Assc Natl Joint Registry Terminated
New England Bapt Hospital Joint Registry Terminated


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

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