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BX SONIC BALLOON EXPANDABLE STENT OTW DELIVERY SYSTEM

FDA premarket approval P900043/S030 · decided 2002-04-29

Approval details

PMA number
P900043
Supplement
S030
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
2001-11-05
Decision date
2002-04-29
Days to decision
175 days
Decision code
APPR
Product code
MAF
Advisory committee
Cardiovascular
Expedited review
No
Location
Miami Lakes, FL
Statement
APPROVAL 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; AND 2) FOR TREATMENT OF ABRUPT OR THREATENED VESSEL CLOSURE IN PATIENTS WITH FAILED INTERVENTIONAL THERAPY IN LES

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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