Kyphoplasty systems

Bone Tamp

by Sontec Instruments, 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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Bone Tamp models and sizes

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

Model / catalog no.SizeMRIStatus
335-400Length 10 in Not statedAvailable
335-404Length 10 in Not statedAvailable
1103-195Length 9.5 in Not statedAvailable
1103-197ALength 8 in Not statedAvailable
1103-197BLength 8 in Not statedAvailable
1103-197CLength 8 in Not statedAvailable

Procedures that use kyphoplasty systems

Frequently asked questions

What is Bone Tamp 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 Bone Tamp?

Bone Tamp is made by Sontec Instruments, Inc.. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.

What sizes does Bone Tamp come in?

Sizes listed for Bone Tamp: Length: 8–10 in. Confirm availability with the manufacturer's instructions for use.

Is Bone Tamp MRI safe?

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

Is Bone Tamp FDA cleared?

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

How do I contact a Sontec Instruments, Inc. sales representative?

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