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RAPTORAIL PTCA DILATATION CATHETER

FDA premarket approval P880003/S082 · decided 2001-09-27

Approval details

PMA number
P880003
Supplement
S082
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
RAPTORAIL PTCA DILATATION CATHETER
Generic name
Catheters, transluminal coronary angioplasty, percutaneous
Applicant
Cordis Corp.
Date received
2001-04-02
Decision date
2001-09-27
Days to decision
178 days
Decision code
APPR
Product code
LOX
Advisory committee
Cardiovascular
Expedited review
No
Location
Miami Lakes, FL
Statement
APPROVAL FOR A NEW CATHETER MODEL. THE DEVICE, AS MODIFIED, WILL BE MARKETED UNDER THE TRADE NAME RAPTORAIL(TM) PTCA DILATATION CATHETER AND IS INDICATED FOR BALLOON DILATATION OF THE STENOTIC PORTION OF A CORONARY ARTERY OR BYPASS GRAFT STENOSIS FOR THE PURPOSE OF IMPROVING MYOCARDIAL PERFUSION.

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