Carotid stents
Neuroguard IEP System
A sterile, non-drug-eluting, flexible tube designed for percutaneous transluminal angioplasty (PTA) to dilate a stenotic peripheral (i.e., non-cerebral, non-coronary) artery by controlled inflation of a distensible balloon(s) at its distal tip; it may also be intended for positioning and expansion of a stent/stent-graft. It is available as an over-the-wire (OTW) type with multiple lumens, or a rapid exchange (RX) type with a single lumen. Some types may include cutting/scoring elements (e.g., microsurgical blades, dual wire configurations) to score/modify the plaque. This is a single-use device.
Find similar vascular stents
Where to buy Neuroguard IEP System
We do not have contact details for Contego Medical, Inc. yet. Send a request and we will route it to the right person for your country.
Neuroguard IEP System models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| NG-0630-140-2 | — | MR Conditional | Available |
| NG-0640-140-2 | — | MR Conditional | Available |
| NG-0730-140-2 | — | MR Conditional | Available |
| NG-0740-140-2 | — | MR Conditional | Available |
| NG-NV-6-30 | — | MR Conditional | Available |
| NG-NV-6-40 | — | MR Conditional | Available |
| NG-NV-7-30 | — | MR Conditional | Available |
| NG-NV-7-40 | — | MR Conditional | Available |
FDA clearances
- PMA P240009 November 2024
Procedures that use carotid stents
Frequently asked questions
What is Neuroguard IEP System used for?
A sterile, non-drug-eluting, flexible tube designed for percutaneous transluminal angioplasty (PTA) to dilate a stenotic peripheral (i.e., non-cerebral, non-coronary) artery by controlled inflation of a distensible balloon(s) at its distal tip; it may also be intended for positioning and expansion of a stent/stent-graft. It is available as an over-the-wire (OTW) type with multiple lumens, or a rapid exchange (RX) type with a single lumen. Some types may include cutting/scoring elements (e.g., microsurgical blades, dual wire configurations) to score/modify the plaque. This is a single-use device.
Who makes Neuroguard IEP System?
Neuroguard IEP System is made by Contego Medical, Inc.. It is listed under carotid stents in our device library.
What sizes does Neuroguard IEP System come in?
The FDA device database does not list sizes for Neuroguard IEP System. Check the instructions for use or ask a Contego Medical, Inc. representative.
Is Neuroguard IEP System MRI safe?
The FDA device database lists Neuroguard IEP System as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Neuroguard IEP System FDA cleared?
Neuroguard IEP System is covered by FDA submission P240009.
How do I contact a Contego Medical, Inc. sales representative?
Contego Medical, Inc. has not listed representatives on LA Vascular yet. Visit the Contego Medical, Inc. company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.