Atlas FDA

Scoreflex NC

FDA premarket approval P200041/S001 · decided 2023-06-29

Approval details

PMA number
P200041
Supplement
S001
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Scoreflex NC
Generic name
Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring
Applicant
OrbusNeich Medical (Shenzhen) Co., Ltd.
Date received
2023-05-18
Decision date
2023-06-29
Days to decision
42 days
Decision code
OK30
Product code
NWX
Advisory committee
Cardiovascular
Expedited review
No
Location
Shenzhen
Statement
Addition of a new manufacturing location for the manufacture of select components of the final Scroreflex NC device.

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510(k) clearances by this applicant

RecordFirmDate
Teleport Glide Microcatheter (K253361)OrbusNeich Medical (Shenzhen) Co., Ltd.2026-04-10
COREPASS Modular Microcatheter (FLEX); COREPASS Modular Microcatheter (CONTROL) (K242588)OrbusNeich Medical (Shenzhen) Co., Ltd.2025-01-07
Sapphire NC ULTRA Coronary Dilatation Catheter (K233499)OrbusNeich Medical (Shenzhen) Co., Ltd.2024-08-16
Sapphire ULTRA Coronary Dilatation Catheter (K233505)OrbusNeich Medical (Shenzhen) Co., Ltd.2024-08-15
JADE PLUS PTA Balloon Dilatation Catheter (K241025)OrbusNeich Medical (Shenzhen) Co., Ltd.2024-06-11
Teleport XT Microcatheter (K231608)OrbusNeich Medical (Shenzhen) Co., Ltd.2024-01-07
Sapphire NC 24 (K211807)OrbusNeich Medical (Shenzhen) Co., Ltd.2021-10-14
JADE (K202231)OrbusNeich Medical (Shenzhen) Co., Ltd.2020-12-10