Kyphoplasty systems

GraftMag Graft Delivery System

by Spine Wave, 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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GraftMag Graft Delivery System models and sizes

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

Model / catalog no.SizeMRIStatus
10-7506— Not statedAvailable
10-7507— Not statedAvailable
10-7519— Not statedAvailable

Procedures that use kyphoplasty systems

Frequently asked questions

What is GraftMag Graft Delivery System 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 GraftMag Graft Delivery System?

GraftMag Graft Delivery System is made by Spine Wave, Inc.. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.

What sizes does GraftMag Graft Delivery System come in?

The FDA device database does not list sizes for GraftMag Graft Delivery System. Check the instructions for use or ask a Spine Wave, Inc. representative.

Is GraftMag Graft Delivery System MRI safe?

The FDA device database entry for GraftMag Graft Delivery System does not state its MRI safety status. Check the labeling before MRI.

Is GraftMag Graft Delivery System FDA cleared?

GraftMag Graft Delivery System is registered in the FDA's Global Unique Device Identification Database (GUDID).

How do I contact a Spine Wave, Inc. sales representative?

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