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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.
 
DeviceEXABLATE
Classification Nameablation system, high intensity focused ultrasound (hifu), mr-guided
Generic Nameablation system, high intensity focused ultrasound (hifu), mr-guided
Applicant
INSIGHTEC, LTD
4851 lbj frwy, ste 400
dallas, TX 75244
PMA NumberP040003
Supplement NumberS008
Date Received07/01/2010
Decision Date08/23/2010
Product Code
NRZ[ Registered Establishments with NRZ ]
Advisory Committee Obstetrics/Gynecology
Supplement Typereal-time process
Supplement Reason change design/components/specifications/material
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
APPROVAL FOR SOFTWARE CHANGES INCLUDED IN VERSION 4.24 OF THE WORK STATION SOFTWARE.
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