Kyphoplasty systems

General Instrument

by Orthopediatrics Corp.

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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Where to buy General Instrument

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General Instrument models and sizes

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

Model / catalog no.SizeMRIStatus
01-1000-019— Not statedAvailable
01-1000-020— Not statedAvailable

Procedures that use kyphoplasty systems

Frequently asked questions

What is General Instrument 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 General Instrument?

General Instrument is made by Orthopediatrics Corp.. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.

What sizes does General Instrument come in?

The FDA device database does not list sizes for General Instrument. Check the instructions for use or ask a Orthopediatrics Corp. representative.

Is General Instrument MRI safe?

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

Is General Instrument FDA cleared?

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

How do I contact a Orthopediatrics Corp. sales representative?

Orthopediatrics Corp. has not listed representatives on LA Vascular yet. Visit the Orthopediatrics Corp. 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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