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SCIMED RADIUS CORONARY STENT WITH DELIVERY SYSTEM

FDA premarket approval P970061/S001 · decided 1999-02-04

Approval details

PMA number
P970061
Supplement
S001
Supplement type
Normal 180 Day Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
SCIMED RADIUS CORONARY STENT WITH DELIVERY SYSTEM
Applicant
Boston Scientific Scimed, Inc.
Date received
1998-08-10
Decision date
1999-02-04
Days to decision
178 days
Decision code
APPR
Advisory committee
Cardiovascular
Expedited review
No
Location
Maple Grove, MN
Statement
Approval for a modification ot the indications statement to include the treatment of saphenous vein graft lesions. The SCIMED RADIUS(TM) Coronary Stent (14 mm and 20 mm lengths) with Delivery System is indicated for use in patients with symptomaitc ischemic heart disease due to discrete de novo native coronary artery and saphenous vein bypass graft lesions (length <30mm) with reference vessel diamter ranging from 2.75 to 4.25 mm and is intended to improve coronary luminial diameter.

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510(k) clearances by this applicant

RecordFirmDate
MODIFICATION TO ATLANTIS PV IMAGING CATHETER, MODEL 36456 (K041727)Boston Scientific Scimed, Inc.2004-07-23
PT2 GUIDE WIRE AND ADDWIRE EXTENSION WIRE (K030617)Boston Scientific Scimed, Inc.2003-05-21
MODIFICATION TO BOSTON SCIENTIFIC EXPRESS BILIARY LD PREMOUNTED STENT SYSTEM (K024048)Boston Scientific Scimed, Inc.2003-01-06
BOSTON SCIENTIFIC ULTRA-SOFT SV BALLOON DILATATION CATHETER (K021735)Boston Scientific Scimed, Inc.2002-08-08
WALLGRAFT TRACHEOBRONCHIAL ENDOPROTHESIS WITH UNISTEP PLUS DELIVERY SYSTEM (K021901)Boston Scientific Scimed, Inc.2002-07-09
MODIFICIATION TO: BILIARY WALLSTENT ENDOPROSTHEIS WITH MONORAIL DELIVERY SYSTEM, MODEL 71-XXX (K012822)Boston Scientific Scimed, Inc.2001-10-24
NIROYAL BILIARY PREMOUNTED STENT SYSTEM (K012216)Boston Scientific Scimed, Inc.2001-08-17
BOSTON SCIENTIFIC SCIMED ATLANTIS CORONARY IMAGING CATHETER, MODEL C4020 (K000743)Boston Scientific Scimed, Inc.2000-09-06