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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 NameTHORATEC VENTRICULAR ASIST DEVICE
Classification Nameventricular (assisst) bypass
Generic Nameventricular assist device
ApplicantTHORATEC LABORATORIES CORP.
PMA NumberP870072
Supplement NumberS012
Date Received09/25/2000
Decision Date06/01/2001
Product Code
DSQ[ Registered Establishments with DSQ ]
Advisory Committee Cardiovascular
Supplement Typenormal 180 day track
Supplement Reason change design/components/specifications - component
Expedited Review Granted? No
Combination Product No
Recalls CDRH Recalls
Approval Order Statement 
Approval for the addition of the tlc-ii portable pneumatic driver to the thoratec paracorporeal ventricular assist device system. The tlc-ii portable pneumatic driver is intended to be interchangeable with the dual drive console in the (currently approved) thoratec paracorporeal ventricular device system for either bridge to transplant patients or for postcardiotomy recovery patients who are unable to be weaned from cardiopulmonary bypass. The tlc-ii portable pneumatic driver is intended for use either in the hospital or in a medically monitored residence facility. In addition, the tlc-ii portable pneumatic driver can be used to allow suitably qualified patients to take off-site excursions within a two-hour travel radius of the hospital in the company of a trained caregiver.
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