Mini Trek RX Coronary Dilatation Catheter (Including 1.20 MM Size), Mini Trek Otw Coronary Dilatation Catheter (Includin
FDA 510(k) K123279 · Abbott Vascular
510(k) numberK123279
Submission
- Device name
- Mini Trek RX Coronary Dilatation Catheter (Including 1.20 MM Size), Mini Trek Otw Coronary Dilatation Catheter (Includin
- Applicant
- Abbott Vascular
Temecula, CA, US - Received
- October 22, 2012
- Decision date
- January 30, 2013
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- LOX – Catheters, Transluminal Coronary Angioplasty, Percutaneous
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.5100
- Specialty
- Cardiovascular
A PTCA catheter is a device that operates on the principle of hydraulic pressurization applied through an inflatable balloon attached to the distal end.
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|---|---|---|---|
| K261428 | NC Euphora Rapid Exchange Balloon Dilatation CatheterLOX · Traditional | Medtronic Ireland | 08/14/2026SE |
| K261759 | Euphora Rapid Exchange (RX) Balloon Dilatation CatheterLOX · Traditional | Medtronic Ireland | 07/27/2026SE |
| K252116 | Firefighter Pro PTCA Balloon CatheterLOX · Traditional | Shanghai MicroPort Medical (Group) Co., Ltd. | 04/07/2026SE |
| K254022 | FLASH Flex Aorto-Ostial Angioplasty SystemLOX · Traditional | Verge Medical, Inc. | 04/02/2026SE |
| K252295 | RyureiLOX · Traditional | Terumo Corporation | 03/27/2026SE |
| K251970 | Sprinter Legend Rapid Exchange Balloon Dilatation CatheterLOX · Traditional | Medtronic, Ireland | 01/17/2026SE |
| K242969 | Pantera Pro; Pantera LEOLOX · Special | Biotronik, Inc. | 10/25/2024SE |
| K233499 | Sapphire NC ULTRA Coronary Dilatation CatheterLOX · Traditional | OrbusNeich Medical (Shenzhen) Co., Ltd. | 08/16/2024SE |
| K233505 | Sapphire ULTRA Coronary Dilatation CatheterLOX · Traditional | OrbusNeich Medical (Shenzhen) Co., Ltd. | 08/15/2024SE |
| K233729 | Ringer perfusion balloon catheter, 2.00 x 20mm (5881); Ringer perfusion balloon…LOX · Traditional | Vascular Solutions, LLC | 05/31/2024SE |
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| K200144 | HI-TORQUE Steelcore Bare Guide WireDQX · Traditional | 04/08/2020SE |
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| K191173 | Emboshield NAV6 Embolic Protection System, Barewire Filter Delivery WiresNTE · Traditional | 07/25/2019SE |
| K180040 | NC TREK RX Coronary Dilatation Catheter; NC TREK OTW Coronary Dilatation Catheter…LOX · Special | 08/24/2018SE |
| K173795 | HI-TORQUE TurnTrac Guide Wire FamilyDQX · Special | 01/12/2018SE |
| K172394 | Steerable Guide CatheterDRA · Special | 09/06/2017SE |
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Questions and answers
When was Mini Trek RX Coronary Dilatation Catheter (Including 1.20 MM Size), Mini Trek Otw Coronary Dilatation Catheter (Includin cleared by the FDA?
Mini Trek RX Coronary Dilatation Catheter (Including 1.20 MM Size), Mini Trek Otw Coronary Dilatation Catheter (Includin (K123279) received a 510(k) decision of Substantially Equivalent on January 30, 2013, 100 days after the submission was received.
What is the product code of K123279?
The FDA product code is LOX – Catheters, Transluminal Coronary Angioplasty, Percutaneous, a Class II (moderate risk) device regulated under 21 CFR 870.5100.