Atlas FDA

Lacrosse NSE ALPHA Coronary Dilatation Catheter

FDA premarket approval P230026/S005 · decided 2026-07-22

Approval details

PMA number
P230026
Supplement
S005
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Lacrosse NSE ALPHA Coronary Dilatation Catheter
Generic name
Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring
Applicant
Goodman Co., Ltd.
Date received
2026-06-22
Decision date
2026-07-22
Days to decision
30 days
Decision code
OK30
Product code
NWX
Advisory committee
Cardiovascular
Expedited review
No
Location
Nagoya
Statement
endotoxin equipment and testing methodology changes

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510(k) clearances by this applicant

RecordFirmDate
Aperta NSE PTA Balloon Dilatation Catheter (K243944)Goodman Co., Ltd.2025-04-22
Aperta NSE PTA Balloon Dilatation Catheter (AW18-05040040/AA18-05040040, AW18-09040040/AA18-09040040, AW18-14540040, AW18-05050040/AA18-05050040, AW18-09050040/AA18-09050040, AW18-14550040, AW18-05060040/AA18-05060040, AW18-09060040/AA18-09060040, AW18-14560040 AW18-05070040/AA18-05070040, AW18-09070040/AA18-09070040, AW18-14570040, AW18-05080040/AA18-05080040, AW18-09080040/AA18-09080040, AW18-14580040) (K232013)Goodman Co., Ltd.2024-03-28
GOODNET (K010763)Goodman Co., Ltd.2001-05-25