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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.
 
DeviceLITHOTRON ULTRA LITHOSTRIPSY SYSTEM
Generic NameLithotriptor, extracorporeal shock-wave, urological
Regulation Number876.5990
ApplicantHealthtronics Surgical Services, Inc.
425 Franklin Rd., Suite 545
Marietta, GA 30067
PMA NumberP970019
Supplement NumberS004
Date Received08/27/1998
Decision Date09/11/1998
Reclassified Date09/08/2000
Product Code LNS 
Advisory Committee Gastroenterology/Urology
Supplement TypeReal-Time Process
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
Approval for the following modifications to the LithoTron(TM) Lithotripsy System: 1) replacement of the transportable C-arm fluoroscopy system with an upgraded, stationary x-ray imaging system, 2) replacement of the existing patient table with one that offers Trendelenburg positioning, and 3) the addition of motorized movement of the shock wave therapy head. The device is indicated for use in patients with renal and upper ureteral calculi between 4mm and 20mm in size.
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