Atlas FDA

AngioSculpt Evo RX PTCA Scoring Balloon Catheter with Hydrophilic Coating

FDA premarket approval P050018/S034 · decided 2024-02-14

Approval details

PMA number
P050018
Supplement
S034
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
AngioSculpt Evo RX PTCA Scoring Balloon Catheter with Hydrophilic Coating
Generic name
Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring
Applicant
Spectranetics Corp.
Date received
2023-11-13
Decision date
2024-02-14
Days to decision
93 days
Decision code
APPR
Product code
NWX
Advisory committee
Cardiovascular
Expedited review
No
Location
Fremont, CA
Statement
approval for a manufacturing site located at Creganna Medical S.L.R, San Rafael, Costa Rica to manufacture the base catheter

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