Kyphoplasty systems
Sq.line
by Aesculap AG
A hand-held, surgical instrument designed to be used to manually pack tissue or other material during a surgical intervention. It typically consists of a shaft that terminates in a blunt (flat or profiled) tip at the distal end and a handle at the proximal end. It is typically a one-piece instrument made of metal, however some types may employ a synthetic material for the handle (e.g., Tufnol). The surgeon may pack the material by applying hand pressure to the device or by tapping the proximal end with a hammer/mallet. This is a reusable device.
Where to buy Sq.line
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Sq.line 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 |
|---|---|---|---|
| ND584NR | — | Not stated | Available |
| ND585NR | — | Not stated | Available |
| ND586NR | — | Not stated | Available |
| ND587NR | — | Not stated | Available |
| ND588NR | — | Not stated | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is Sq.line used for?
A hand-held, surgical instrument designed to be used to manually pack tissue or other material during a surgical intervention. It typically consists of a shaft that terminates in a blunt (flat or profiled) tip at the distal end and a handle at the proximal end. It is typically a one-piece instrument made of metal, however some types may employ a synthetic material for the handle (e.g., Tufnol). The surgeon may pack the material by applying hand pressure to the device or by tapping the proximal end with a hammer/mallet. This is a reusable device.
Who makes Sq.line?
Sq.line is made by Aesculap AG. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does Sq.line come in?
The FDA device database does not list sizes for Sq.line. Check the instructions for use or ask a Aesculap AG representative.
Is Sq.line MRI safe?
The FDA device database entry for Sq.line does not state its MRI safety status. Check the labeling before MRI.
Is Sq.line FDA cleared?
Sq.line is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Aesculap AG sales representative?
Aesculap AG has not listed representatives on LA Vascular yet. Visit the Aesculap AG 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.