Kyphoplasty systems

Elemax Cortical Cancellous Spacer

by Rti Surgical, Inc.

A collection of instruments and devices intended to be used for the placement of an internal orthopaedic fixation system into or onto all types of bones (e.g., bones of limbs, spine, pelvis, or craniomaxillofacial). It is a non-dedicated device that includes various metallic and/or plastic reusable devices [e.g., retractors, rods, clamps, drills, pins, saws, screwdrivers, guides, trials, impactors] intended to be used for the implantation of any type of internal orthopaedic fixation system; the implant(s) is not included. This is a reusable device.

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Elemax Cortical Cancellous Spacer models and sizes

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

Model / catalog no.SizeMRIStatus
723-643— Not statedAvailable
723-917— Not statedAvailable

Procedures that use kyphoplasty systems

Frequently asked questions

What is Elemax Cortical Cancellous Spacer used for?

A collection of instruments and devices intended to be used for the placement of an internal orthopaedic fixation system into or onto all types of bones (e.g., bones of limbs, spine, pelvis, or craniomaxillofacial). It is a non-dedicated device that includes various metallic and/or plastic reusable devices [e.g., retractors, rods, clamps, drills, pins, saws, screwdrivers, guides, trials, impactors] intended to be used for the implantation of any type of internal orthopaedic fixation system; the implant(s) is not included. This is a reusable device.

Who makes Elemax Cortical Cancellous Spacer?

Elemax Cortical Cancellous Spacer is made by Rti Surgical, Inc.. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.

What sizes does Elemax Cortical Cancellous Spacer come in?

The FDA device database does not list sizes for Elemax Cortical Cancellous Spacer. Check the instructions for use or ask a Rti Surgical, Inc. representative.

Is Elemax Cortical Cancellous Spacer MRI safe?

The FDA device database entry for Elemax Cortical Cancellous Spacer does not state its MRI safety status. Check the labeling before MRI.

Is Elemax Cortical Cancellous Spacer FDA cleared?

Elemax Cortical Cancellous Spacer is registered in the FDA's Global Unique Device Identification Database (GUDID).

How do I contact a Rti Surgical, Inc. sales representative?

Rti Surgical, Inc. has not listed representatives on LA Vascular yet. Visit the Rti Surgical, 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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