Kyphoplasty systems

Fusion Posterior Instrument Set

by Xtant Medical Holdings, 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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Fusion Posterior Instrument Set models and sizes

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

Model / catalog no.SizeMRIStatus
30-TAMP-L— Not statedAvailable
30-TAMP-S— Not statedAvailable

Procedures that use kyphoplasty systems

Frequently asked questions

What is Fusion Posterior Instrument Set 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 Fusion Posterior Instrument Set?

Fusion Posterior Instrument Set is made by Xtant Medical Holdings, Inc.. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.

What sizes does Fusion Posterior Instrument Set come in?

The FDA device database does not list sizes for Fusion Posterior Instrument Set. Check the instructions for use or ask a Xtant Medical Holdings, Inc. representative.

Is Fusion Posterior Instrument Set MRI safe?

The FDA device database entry for Fusion Posterior Instrument Set does not state its MRI safety status. Check the labeling before MRI.

Is Fusion Posterior Instrument Set FDA cleared?

Fusion Posterior Instrument Set is registered in the FDA's Global Unique Device Identification Database (GUDID).

How do I contact a Xtant Medical Holdings, Inc. sales representative?

Xtant Medical Holdings, Inc. has not listed representatives on LA Vascular yet. Visit the Xtant Medical Holdings, 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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