Kyphoplasty systems

Harmony Posterior Instruments

by Highridge Medical, LLC

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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Harmony Posterior Instruments models and sizes

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

Model / catalog no.SizeMRIStatus
2755-1— Not statedAvailable

Procedures that use kyphoplasty systems

Frequently asked questions

What is Harmony Posterior Instruments 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 Harmony Posterior Instruments?

Harmony Posterior Instruments is made by Highridge Medical, LLC. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.

What sizes does Harmony Posterior Instruments come in?

The FDA device database does not list sizes for Harmony Posterior Instruments. Check the instructions for use or ask a Highridge Medical, LLC representative.

Is Harmony Posterior Instruments MRI safe?

The FDA device database entry for Harmony Posterior Instruments does not state its MRI safety status. Check the labeling before MRI.

Is Harmony Posterior Instruments FDA cleared?

Harmony Posterior Instruments is registered in the FDA's Global Unique Device Identification Database (GUDID).

How do I contact a Highridge Medical, LLC sales representative?

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