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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.
 
DeviceNIROYAL(TM1) ELITE PREMOUNTED STENT SYSTEM
ApplicantBoston Scientific Corp
One Boston Scientific Pl.
Natick,, MA 01760
PMA NumberP980001
Supplement NumberS017
Date Received02/23/2000
Decision Date08/03/2000
Withdrawal Date08/13/2007
Advisory Committee Cardiovascular
Supplement TypeNormal 180 Day Track
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
APPROVAL FOR THE NIROYAL(TM) ELITE PROMOUNTED STENT SYSTEMS. THE DEVICE IS INDICATED FOR IMPROVING CORONARY LUMINAL DIAMETER IN THE FOLLOWING: *PATIENTS WITH SYMOPTOMATIC ISCHEMIC DISEASE DUE TO DISCRETE DE NOVO LESIONS IN NATIVE CORONARY ARTERIES (LENGTH <= 25 MM) WITH A REFERENCE VESSEL DIAMETER OF 3.0 TO 4.0 MM; * TREATMENT OF ABRUPT OR THREATENED CLOSURE IN PATIENTS WITH FAILED IN TERVENTIONAL THERAPY IN LESIONS WITH REFERENCE DIAMETERS IN THE RANGE OF 2.5 TO 4.0 MM; AND * PATIENTS WITH SYMPTOMATIC HEART DISEASE DUE TO LESIONS IN SAPHENOUS VEIN BYPASS GRAFTS WITH LESION LENGTH <= 30 MM AND REFERENCE DIAMETER IN THE RANGE OF 3.0 TO 4.0 MM.
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