Atlas FDA

AngioSculpt® Evo RX PTCA Scoring Balloon Catheter with Hydrophilic Coating

FDA premarket approval P050018/S033 · decided 2023-10-19

Approval details

PMA number
P050018
Supplement
S033
Supplement type
30-Day Notice
Supplement reason
Process 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
2023-09-19
Decision date
2023-10-19
Days to decision
30 days
Decision code
OK30
Product code
NWX
Advisory committee
Cardiovascular
Expedited review
No
Location
Fremont, CA
Statement
alternate Tier III supplier for raw material used in the hydrophilic coating

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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