Kyphoplasty systems
Coveris
by Camber Spine Technologies, 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.
Where to buy Coveris
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Coveris models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| CS-107-253 | — | Not stated | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is Coveris 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 Coveris?
Coveris is made by Camber Spine Technologies, LLC. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does Coveris come in?
The FDA device database does not list sizes for Coveris. Check the instructions for use or ask a Camber Spine Technologies, LLC representative.
Is Coveris MRI safe?
The FDA device database entry for Coveris does not state its MRI safety status. Check the labeling before MRI.
Is Coveris FDA cleared?
Coveris is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Camber Spine Technologies, LLC sales representative?
Camber Spine Technologies, LLC has not listed representatives on LA Vascular yet. Visit the Camber Spine Technologies, 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.