Guidewires
Synchro 2
A long, thin, sterile wire intended to be percutaneously placed into the cardiac vasculature (ventricles or coronary vessels) to function as a guide for the introduction, positioning, and/or operation of a device (e.g., catheter, pacing lead); it may also be used in the peripheral vasculature. It may be made of metal (e.g., stainless steel, Nitinol), or polymer and/or glass materials to provide MRI-compatibility, with or without coating, and is available in a variety of distal tip designs. It is used for various diagnostic and interventional procedures, and may include devices used to facilitate manipulation (e.g., torque device). This is a single-use device.
Synchro 2 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 |
|---|---|---|---|
| M00326010 | Outer Diameter 0.014 in; Length 200.0 cm | Not stated | Available |
| M00326110 | Length 200.0 cm; Outer Diameter 0.014 in | Not stated | Available |
| M00326310 | Length 300.0 cm; Outer Diameter 0.014 in | Not stated | Available |
| M00326320 | Length 300.0 cm; Outer Diameter 0.014 in | Not stated | Available |
| M00326410 | Length 200.0 cm; Outer Diameter 0.014 in | Not stated | Available |
| M00326420 | Outer Diameter 0.014 in; Length 200.0 cm | Not stated | Available |
| M00326510 | Outer Diameter 0.014 in; Length 300.0 cm | Not stated | Available |
| M00326520 | Outer Diameter 0.014 in; Length 300.0 cm | Not stated | Available |
FDA clearances
- 510(k) K053268 March 2006
Procedures that use guidewires
Frequently asked questions
What is Synchro 2 used for?
A long, thin, sterile wire intended to be percutaneously placed into the cardiac vasculature (ventricles or coronary vessels) to function as a guide for the introduction, positioning, and/or operation of a device (e.g., catheter, pacing lead); it may also be used in the peripheral vasculature. It may be made of metal (e.g., stainless steel, Nitinol), or polymer and/or glass materials to provide MRI-compatibility, with or without coating, and is available in a variety of distal tip designs. It is used for various diagnostic and interventional procedures, and may include devices used to facilitate manipulation (e.g., torque device). This is a single-use device.
Who makes Synchro 2?
Synchro 2 is made by Stryker Corporation. It is listed under guidewires in our device library.
What sizes does Synchro 2 come in?
Sizes listed for Synchro 2: Outer Diameter: 0.01 in; Length: 200–300 cm. Confirm availability with the manufacturer's instructions for use.
Is Synchro 2 MRI safe?
The FDA device database entry for Synchro 2 does not state its MRI safety status. Check the labeling before MRI.
Is Synchro 2 FDA cleared?
Synchro 2 is covered by FDA submission K053268.
How do I contact a Stryker Corporation sales representative?
Stryker Corporation has not listed representatives on LA Vascular yet. Visit the Stryker Corporation 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.