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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
Trade NameDURASEAL DURAL SEALANT SYSTEM
Classification Namesealant, dural
Generic Namesurgical sealant,polymerizing
ApplicantCOVIDIEN
PMA NumberP040034
Supplement NumberS019
Date Received12/23/2010
Decision Date01/20/2011
Product Code
NQR[ Registered Establishments with NQR ]
Advisory Committee Neurology
Supplement Type Special Supplement
Supplement Reason labeling change - instructions
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for a modification to your instructions for use to instruct the surgeon in the best practices in applying the sealant.
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