Atlas FDA

ANGIOSCULPT(R) PTCA SCORING BALLOON CATHETER

FDA premarket approval P050018/S022 · decided 2016-09-06

Approval details

PMA number
P050018
Supplement
S022
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
ANGIOSCULPT(R) PTCA SCORING BALLOON CATHETER
Generic name
Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring
Applicant
Spectranetics Corp.
Date received
2016-06-08
Decision date
2016-09-06
Days to decision
90 days
Decision code
APPR
Product code
NWX
Advisory committee
Cardiovascular
Expedited review
No
Location
Fremont, CA
Statement
Approval for a non-patient contacting material change for a component of the AngioSculpt PTCA Scoring Balloon Catheter.

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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