Microcatheters
Sendero
A sterile, small-diameter, single-lumen, flexible tube designed for the controlled infusion of fluids (e.g., thrombolytics, diagnostic contrast media) into superselective small vessels (including intracranial, peripheral, or occluded coronary vasculature) for angiography/treatment, and typically also for the delivery of devices (e.g., embolization implants, guidewires) into tortuous vessels or across tight lesions. It may include an ultrasound transducer, a thermal sensor, and a hole for guidewire placement located at the distal tip. It is not a guide-catheter (i.e., is not intended to deliver other catheters or therapeutic leads directly through its lumen). This is a single-use device.
Sendero 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 |
|---|---|---|---|
| SENDERO-MC29-130 | — | Not stated | Available |
FDA clearances
- 510(k) K240384 March 2024
Procedures that use microcatheters
Frequently asked questions
What is Sendero used for?
A sterile, small-diameter, single-lumen, flexible tube designed for the controlled infusion of fluids (e.g., thrombolytics, diagnostic contrast media) into superselective small vessels (including intracranial, peripheral, or occluded coronary vasculature) for angiography/treatment, and typically also for the delivery of devices (e.g., embolization implants, guidewires) into tortuous vessels or across tight lesions. It may include an ultrasound transducer, a thermal sensor, and a hole for guidewire placement located at the distal tip. It is not a guide-catheter (i.e., is not intended to deliver other catheters or therapeutic leads directly through its lumen). This is a single-use device.
Who makes Sendero?
Sendero is made by Okami Medical, Inc.. It is listed under microcatheters in our device library.
What sizes does Sendero come in?
The FDA device database does not list sizes for Sendero. Check the instructions for use or ask a Okami Medical, Inc. representative.
Is Sendero MRI safe?
The FDA device database entry for Sendero does not state its MRI safety status. Check the labeling before MRI.
Is Sendero FDA cleared?
Sendero is covered by FDA submission K240384.
How do I contact a Okami Medical, Inc. sales representative?
Okami Medical, Inc. has not listed representatives on LA Vascular yet. Visit the Okami 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.