Kyphoplasty systems

Endoskeleton Tl

by Medtronic Sofamor Danek, Inc.

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.

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Endoskeleton Tl models and sizes

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

Model / catalog no.SizeMRIStatus
7200-1010Length 12 in Not statedAvailable
7200-1054Length 12 in Not statedAvailable

Procedures that use kyphoplasty systems

Frequently asked questions

What is Endoskeleton Tl 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 Endoskeleton Tl?

Endoskeleton Tl is made by Medtronic Sofamor Danek, Inc.. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.

What sizes does Endoskeleton Tl come in?

Sizes listed for Endoskeleton Tl: Length: 12 in. Confirm availability with the manufacturer's instructions for use.

Is Endoskeleton Tl MRI safe?

The FDA device database entry for Endoskeleton Tl does not state its MRI safety status. Check the labeling before MRI.

Is Endoskeleton Tl FDA cleared?

Endoskeleton Tl is registered in the FDA's Global Unique Device Identification Database (GUDID).

How do I contact a Medtronic Sofamor Danek, Inc. sales representative?

Medtronic Sofamor Danek, Inc. has not listed representatives on LA Vascular yet. Visit the Medtronic Sofamor Danek, 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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