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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 PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DeviceTHORATEC HEARTMATE II LVAS
Classification Nameventricular (assisst) bypass
Generic Nameventricular (assisst) bypass
Applicant
THORATEC CORP.
6035 stoneridge dr.
pleasanton, CA 94588
PMA NumberP060040
Supplement NumberS004
Date Received12/24/2008
Decision Date12/04/2009
Product Code
DSQ[ Registered Establishments with DSQ ]
Advisory Committee Cardiovascular
Supplement Typenormal 180 day track
Supplement Reason change design/components/specifications/material
Expedited Review Granted? No
Combination Product No
Recalls CDRH Recalls
Approval Order Statement 
APPROVAL FOR A NEW SEALED (GELWEAVE) OUTFLOW GRAFT WITH BEND RELIEF FOR USE WITH THE HEARTMATE II LVAS.
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