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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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Note: this medical device has supplements. The device description may have changed. Be sure to look at the supplements to get an up-to-date view of this device.
 
Trade NameARTEGRAFT{TM} AND REINFORCED ARTEGRAFT{TM}
Classification Nametissue graft of 6mm and greater
Generic Nametissue graft of 6mm and greater
ApplicantARTEGRAFT, INC.
PMA NumberN16837
Date Received07/01/1979
Decision Date08/01/1979
Product Code
LXA[ Registered Establishments with LXA ]
Advisory Committee Cardiovascular
Expedited Review Granted? No
Combination Product No
Supplements: S001 S003 S004 S005 S006 S007 
S008 S009 S010 
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