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BX SONIC BALLOON EXPANDABLE STENT OTW DELIVERY SYSTEM

FDA premarket approval P900043/S038 · decided 2002-08-02

Approval details

PMA number
P900043
Supplement
S038
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
BX SONIC BALLOON EXPANDABLE STENT OTW DELIVERY SYSTEM
Generic name
STENT, CORONARY
Applicant
Cordis Corp.
Date received
2002-02-25
Decision date
2002-08-02
Days to decision
158 days
Decision code
APPR
Product code
MAF
Advisory committee
Cardiovascular
Expedited review
No
Location
Miami Lakes, FL
Statement
APPROVAL FOR A MODIFICATION OF THE INDICATIONS FOR THE BX SONIC BALLOON-EXPANDABLE STENT OTW DELIVERY SYSTEM. THE DEVICE, AS MODIFIED, IS INDICATED FOR IMPROVING CORONARY LUMINAL DIAMETER IN THE FOLLOWING: 1) FOR TREATMENT OF PATIENTS WITH SYMPTOMATIC ISCHEMIC HEART DISEASE DUE TO DISCRETE DE NOVO OR RESTENOTIC LESIONS (<=30 MM IN LENGTH) IN NATIVE CORONARY ARTERIES WITH REFERENCE DIAMETERS RANGING FROM 3.0 MM TO 5.0 MM INVOLVING DIRECT STENTING OR PREDILATATION; AND 2) FOR TREATMENT OF ABRUPT O

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510(k) clearances by this applicant

RecordFirmDate
FLEXSTENT BILIARY SELF EXPANDING STENT SYSTEM; S.M.A.R.T. RE-FLEX BILIARY ELF-EXPANDING STENT SYSTEM (K130981)Cordis Corp.2014-03-12
POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER (K112797)Cordis Corp.2012-05-04
ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE, ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE (K101651)Cordis Corp.2010-07-09
MICRO GUIDE CATHETER XP (K082143)Cordis Corp.2008-08-25
SMART NITINOL SELF-EXPANDING STENT, MODEL C06120MB, C07120MB, C08120MB, C06150MB, C07150MB, C08150MB (K062798)Cordis Corp.2008-02-06
PALMAZ BLUE .014 TRANSHEPATIC BILIARY STENT SYSTEM-MODEL PB1550,BAS,BAX,PB1560,BAS,BAX,PB1850,BAS,BAXPB1860BAS,BAX (K060877)Cordis Corp.2006-04-27
CORDIS AMIIA .014 PTA BALLOON CATHETER (K050645)Cordis Corp.2005-04-01
CORDIS STEER-IT DEFLECTING TIP GUIDEWIRE (K040592)Cordis Corp.2004-12-17