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ANGIOSCULPT SCORING BALLOON CATHETER

FDA premarket approval P050018 · decided 2007-01-08

Approval details

PMA number
P050018
Trade name
ANGIOSCULPT SCORING BALLOON CATHETER
Generic name
Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring
Applicant
Spectranetics Corp.
Date received
2005-05-11
Decision date
2007-01-08
Days to decision
607 days
Decision code
APPR
Product code
NWX
Advisory committee
Cardiovascular
Expedited review
No
Location
Fremont, CA
Statement
APPROVAL FOR THE ANGIOSCULPT SCORING BALLOON CATHETER. THE DEVICE IS INDICATED FOR THE TREATMENT OF HEMODYNAMICALLY SIGNIFICANT CORONARY ARTERY STENOSIS, INCLUDING IN-STENT RESTENOSIS AND COMPLEX TYPE C LESIONS, FOR THE PURPOSE OF IMPROVING MYOCARDIAL PERFUSION.

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