Kyphoplasty systems

Brickyard ALIF

by Altus Spine, LLC

A surgical instrument designed to facilitate the correct orientation (alignment) of an orthopaedic fixation implant, implants, or system of implants during orthopaedic surgery. It may be used, e.g., to align a series of bone screws in an implant system for posterior stabilization of the spine, or to align a spinal anatomical fixation implant. It is available in a variety of shapes and sizes and allows the surgeon to engage this device with the implant(s) and align them in the desired configuration. It is typically made of high-grade stainless steel or titanium alloy and will have profiled features to fit into the implant(s) to align them. This is a reusable device.

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Brickyard ALIF models and sizes

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

Model / catalog no.SizeMRIStatus
1030-0040— Not statedAvailable

FDA clearances

  • 510(k) K182406 February 2019

Procedures that use kyphoplasty systems

Frequently asked questions

What is Brickyard ALIF used for?

A surgical instrument designed to facilitate the correct orientation (alignment) of an orthopaedic fixation implant, implants, or system of implants during orthopaedic surgery. It may be used, e.g., to align a series of bone screws in an implant system for posterior stabilization of the spine, or to align a spinal anatomical fixation implant. It is available in a variety of shapes and sizes and allows the surgeon to engage this device with the implant(s) and align them in the desired configuration. It is typically made of high-grade stainless steel or titanium alloy and will have profiled features to fit into the implant(s) to align them. This is a reusable device.

Who makes Brickyard ALIF?

Brickyard ALIF is made by Altus Spine, LLC. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.

What sizes does Brickyard ALIF come in?

The FDA device database does not list sizes for Brickyard ALIF. Check the instructions for use or ask a Altus Spine, LLC representative.

Is Brickyard ALIF MRI safe?

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

Is Brickyard ALIF FDA cleared?

Brickyard ALIF is covered by FDA submission K182406.

How do I contact a Altus Spine, LLC sales representative?

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