Kyphoplasty systems

Compression Staple System

by Tornier, Inc.

A hand-held manual surgical instrument designed to strike a surface or another device (e.g., a surgical chisel, gouge, driver) to drive it during a surgical intervention. It is available in a variety of designs and materials; the shaft is typically made of metal (e.g., chromed iron (Fe) or high-grade stainless steel), but can be made of synthetic materials (e.g., Tufnol), and tapers distally to the head. The head is typically a solid, cylindrical shape normally being double-ended and made of solid (iron/steel) or shock-absorbing materials (e.g., rubber, plastic, or Tufnol). Also referred to as a surgical hammer it may also be used for autopsy. This is a reusable device.

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Compression Staple System models and sizes

From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.

Model / catalog no.SizeMRIStatus
STP-054ML— Not statedAvailable
STP-054S— Not statedAvailable

Procedures that use kyphoplasty systems

Frequently asked questions

What is Compression Staple System used for?

A hand-held manual surgical instrument designed to strike a surface or another device (e.g., a surgical chisel, gouge, driver) to drive it during a surgical intervention. It is available in a variety of designs and materials; the shaft is typically made of metal (e.g., chromed iron (Fe) or high-grade stainless steel), but can be made of synthetic materials (e.g., Tufnol), and tapers distally to the head. The head is typically a solid, cylindrical shape normally being double-ended and made of solid (iron/steel) or shock-absorbing materials (e.g., rubber, plastic, or Tufnol). Also referred to as a surgical hammer it may also be used for autopsy. This is a reusable device.

Who makes Compression Staple System?

Compression Staple System is made by Tornier, Inc.. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.

What sizes does Compression Staple System come in?

The FDA device database does not list sizes for Compression Staple System. Check the instructions for use or ask a Tornier, Inc. representative.

Is Compression Staple System MRI safe?

The FDA device database entry for Compression Staple System does not state its MRI safety status. Check the labeling before MRI.

Is Compression Staple System FDA cleared?

Compression Staple System is registered in the FDA's Global Unique Device Identification Database (GUDID).

How do I contact a Tornier, Inc. sales representative?

Tornier, Inc. has not listed representatives on LA Vascular yet. Visit the Tornier, 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.

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