Atlas FDA

ANGIOSCULPT PTCA SCORING BALLOON CATHETER

FDA premarket approval P050018/S017 · decided 2013-01-10

Approval details

PMA number
P050018
Supplement
S017
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
ANGIOSCULPT PTCA SCORING BALLOON CATHETER
Generic name
Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring
Applicant
Spectranetics Corp.
Date received
2012-05-10
Decision date
2013-01-10
Days to decision
245 days
Decision code
APPR
Product code
NWX
Advisory committee
Cardiovascular
Expedited review
No
Location
Fremont, CA
Statement
APPROVAL FOR A NEW BALLOON LENGTH, AND TO INCORPORATE DESIGN, MANUFACTURING PROCESS AND LABELING CHANGES FOR THE RAPID EXCHANGE (RX) DELIVERY SYSTEM.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

RecordFirmDate
LEXICONTURE MECHANICAL DILATOR SHEATH SET (K140047)Spectranetics Corp.2014-04-09
2.5MM TURBO ELITE 035, 2.3MM TURBO ELITE 035 (K123632)Spectranetics Corp.2013-01-25
8FR TURBO - TANDEM SYSTEM (K112032)Spectranetics Corp.2011-10-17
TORQMAX SHEATH GRIP ACCESSORY (K093257)Spectranetics Corp.2010-03-26
TURBO-TANDEM SYSTEM MODEL 472-110 (K094036)Spectranetics Corp.2010-01-25
SPECTRANETICS VISISHEATH DILATOR SHEATH (K092378)Spectranetics Corp.2009-11-02
SPECTRANETICS QUICK CROSS EXTREME SUPPORT CATHETERS (K092396)Spectranetics Corp.2009-09-04
SPECTRANETICS TURBO-TANDEM SYSTEM (K091299)Spectranetics Corp.2009-07-01