Selethru NC Ptca Balloon Dilatation Catheter

Selethru NC is a rapid-exchange balloon catheter for dilating narrowed coronary arteries or bypass grafts. Its noncompliant balloon expands when an inflation device delivers contrast medium…

Registry build 21.09.26

Selethru NC is a rapid-exchange balloon catheter for dilating narrowed coronary arteries or bypass grafts. Its noncompliant balloon expands when an inflation device delivers contrast medium through the catheter’s inflation pathway.

The proximal shaft is PTFE-coated stainless steel, while the distal assembly contains separate balloon-inflation and guidewire pathways. A hydrophilic coating covers the distal section.

Positioning Features

Two platinum-iridium marker bands identify the balloon segment under fluoroscopy. Proximal shaft markings help gauge position relative to the guiding catheter, and a distal rapid-exchange port permits catheter exchange over a standard guidewire. The 142 cm catheter is supplied sterile for single use and does not provide a separate distal dye-injection lumen.

12manufacturers in China registered for this device type
83catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (4), Guangdong (3), Beijing (2).

Chinese manufacturers registered for FDA product code LOX
Manufacturer City Province Registered as Device types
Steris Sterilization Technologies (Suzhou) Ltd Suzhou Jiangsu Contract manufacturer 44
Goals Sterilization Co., Ltd. Jiaxing Zhejiang Contract manufacturer 26
Wuxi Goals Medical Technology Co., Ltd. Yixing Jiangsu Contract manufacturer 24
Suzhou Prosteri Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 20
Lepu Medical Technology (Beijing) Co., Ltd. Beijing Beijing Manufacturer 7
Beijing Target Medical Technologies Inc. Beijing Beijing Contract manufacturer 7
OrbusNeich Medical (Shenzhen) Co., Ltd. Shenzhen Guangdong Complaint-file establishment 5
Brosmed Medical Co., Ltd. Dongguan Guangdong Contract manufacturer 4
Dongguan TT Medical, Inc. Dongguan Guangdong Manufacturer 4
Kossel Medtech (Suzhou) Co., Ltd. Suzhou Jiangsu Manufacturer 4
Shanghai Microport Medical (Group) Co., Ltd. Shanghai Shanghai Specification developer 1
Sino Medical Sciences Technology Inc. Tianjin Tianjin Manufacturer 1

Record

Regulatory record for Selethru NC Ptca Balloon Dilatation Catheter
Listed by Kossel Medtech (Suzhou) Co., Ltd., China
FDA product code LOX
Device type Catheters, Transluminal Coronary Angioplasty, Percutaneous
Device class Class 2
Regulation 21 CFR 870.5100
Establishment Manufacturer
510(k) K211393
Record published 2021-09-20

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Selethru NC Ptca Balloon Dilatation Catheter
Catalogue number Size Status
KNC200010 In distribution
KNC225012 In distribution
KNC325008 In distribution
KNC400008 In distribution
KNC450012 In distribution
KNC400012 In distribution
KNC300030 In distribution
KNC350030 In distribution
KNC375020 In distribution
KNC500020 In distribution
KNC375015 In distribution
KNC400006 In distribution
KNC400030 In distribution
KNC275012 In distribution
KNC200030 In distribution
KNC375030 In distribution
KNC200015 In distribution
KNC275015 In distribution
KNC275030 In distribution
KNC450020 In distribution
KNC400010 In distribution
KNC275006 In distribution
KNC325012 In distribution
KNC225006 In distribution
KNC450015 In distribution
KNC500012 In distribution
KNC500010 In distribution
KNC250025 In distribution
KNC225020 In distribution
KNC200012 In distribution
KNC225030 In distribution
KNC400015 In distribution
KNC300020 In distribution
KNC375012 In distribution
KNC375010 In distribution
KNC250015 In distribution
KNC225008 In distribution
KNC225025 In distribution
KNC350012 In distribution
KNC350025 In distribution
KNC325015 In distribution
KNC325030 In distribution
KNC275010 In distribution
KNC325025 In distribution
KNC250008 In distribution
KNC300010 In distribution
KNC300008 In distribution
KNC200006 In distribution
KNC500006 In distribution
KNC300006 In distribution
KNC325006 In distribution
KNC250006 In distribution
KNC375006 In distribution
KNC200020 In distribution
KNC375008 In distribution
KNC200008 In distribution
KNC225015 In distribution
KNC350006 In distribution
KNC275008 In distribution
KNC200025 In distribution
KNC325010 In distribution
KNC450008 In distribution
KNC300012 In distribution
KNC250012 In distribution
KNC250010 In distribution
KNC350010 In distribution
KNC375025 In distribution
KNC350008 In distribution
KNC450010 In distribution
KNC300015 In distribution
KNC325020 In distribution
KNC275020 In distribution
KNC275025 In distribution
KNC350015 In distribution
KNC350020 In distribution
KNC250020 In distribution
KNC400020 In distribution
KNC300025 In distribution
KNC250030 In distribution
KNC450006 In distribution
KNC500008 In distribution
KNC400025 In distribution
KNC500015 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
NC Emerge® Boston Scientific Corporation 144
Sprinter® Legend Medtronic, Inc. 133
NC Quantum Apex™ Boston Scientific Corporation 128
Trek Abbott Vascular 120
Emerge™ Boston Scientific Corporation 119
NC Trek Abbott Vascular 118
Apex™ Boston Scientific Corporation 116
Maverick²™ Boston Scientific Corporation 113
Apollo Balloon Dilatation Catheter Brosmed Medical Co., Ltd. 110
Sprinter® Medtronic, Inc. 108
NC Stormer™ OTW Medtronic, Inc. 108
Quantum™ Maverick™ Boston Scientific Corporation 106

Showing 12 of 67. All products under Catheters, Transluminal Coronary Angioplasty, Percutaneous

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K211349 2022-01-07
K211393 2021-07-02
K182699 2018-11-26

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P020037 2003-06-11 FX MINIRAIL RX PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY (PTCA) CATHETER Abbott Vascular
P790017 2003-03-04 NC STORMER OVER-THE-WIRE BALLOON DILATATION CATHETER AND NC STORMER ZIPPER MX BALLOON DILATATION CATHETER Medtronic Ireland
P880027 2002-06-25 PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY (PTCA) Boston Scientific Corporation
P860019 2000-12-08 MAXXUM AND NC MAXXUM PTCA CATHETER Scimed Life Systems, Inc.
P880003 2000-07-07 NINJA FX PTCA DILATATION CATHETER Cordis Corp.
P990008 1999-09-27 COOK MBC PTCA BALLOON DILATATION CATHETER Cook Incorporated
P960014 1998-10-05 MAGELLAN-C PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY(PTCA) CATHETERS MODEL C22020,C22520,C23020,& C23520 Global Therapeutics, Inc.
P970052 1998-04-08 LYNX CONTOUR CORONARY BALLOON DILATATION CATHETER(A NEW MODEL OF THE FACT CATHETER). Endologix LLC
P930012 1997-05-29 THE WRAP(PTCA) CATHETER Progressive Angioplasty Systems, Inc.
P910031 1996-12-02 FACT(TM)AND ARC BALLOON CORNARY DILATATION CATHETERS Abbott Vascular Devices
P890048 1996-11-26 USCI(R) PROBE III(TM) BALLOON-ON-A-WIRE(TM) D. SYS Usci, Div. C.R. Bard, Inc.
P890001 1996-06-07 LEOCOR PICO RUNNER(TM) PTCA CATHETER Leocor, Inc.
P850021 1995-07-12 HYBRID (PTCA) CATHETER Abbott Vascular
P940009 1994-09-29 PERCUTANEUS TRANSLUMINAL CORONARY ANGIOPLASTY CATH Scimed Life Systems, Inc.
P890032 1992-07-23 CORDIS ORION STEERABLE PTCA BALLOON CATHETER Cordis Corp.
P880055 1991-07-19 MICROSS-SL(TM) PTCA DILATATION CATHETER Boston Scientific Corporation
P840040 1991-01-30 HEART TRAK PTCA CATHETER Boston Scientific Corporation
P810046 1990-10-05 ACS RX(R) –.014 CORONARY DILATATION CATHETER Advanced Cardiovascular Systems, Inc.
P870021 1990-10-04 PRIME{TM} MODEL 6520, 6525, 6530 AND 6535 Medtronic, Inc.
P880065 1990-09-19 MANSFIELD SCI. AORTIC VALVULOPLASTY CATHETER Boston Scientific Corporation
P870036 1989-06-23 VERSAFLEX BUCHBINDER OMNIFLEX PTCA CATHETER SYSTEM Medtronics Interventional Vascular

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer