Kyphoplasty systems

TruTrack Memory Staple System

by Intelivation, LLC

A non-powered, hand-held, surgical instrument designed to transmit impact forces, typically from a hammer/mallet to an orthopaedic implant (e.g., intramedullary nail or stem), to position/drive the implant into the body during impact-based implantation. It commonly includes an impact-absorbing handle with a distal end shaped to conform to the implant (i.e., flat or anatomically curved). This is a reusable device.

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Where to buy TruTrack Memory Staple System

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TruTrack Memory 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
2001.17653— Not statedAvailable
2001.17654— Not statedAvailable

Procedures that use kyphoplasty systems

Frequently asked questions

What is TruTrack Memory Staple System used for?

A non-powered, hand-held, surgical instrument designed to transmit impact forces, typically from a hammer/mallet to an orthopaedic implant (e.g., intramedullary nail or stem), to position/drive the implant into the body during impact-based implantation. It commonly includes an impact-absorbing handle with a distal end shaped to conform to the implant (i.e., flat or anatomically curved). This is a reusable device.

Who makes TruTrack Memory Staple System?

TruTrack Memory Staple System is made by Intelivation, LLC. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.

What sizes does TruTrack Memory Staple System come in?

The FDA device database does not list sizes for TruTrack Memory Staple System. Check the instructions for use or ask a Intelivation, LLC representative.

Is TruTrack Memory Staple System MRI safe?

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

Is TruTrack Memory Staple System FDA cleared?

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

How do I contact a Intelivation, LLC sales representative?

Intelivation, LLC has not listed representatives on LA Vascular yet. Visit the Intelivation, LLC 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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