Kyphoplasty systems
Facet
by Seaspine Orthopedics Corporation
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.
Facet 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 |
|---|---|---|---|
| FF2-000003 | — | Not stated | Available |
| FF2-100003 | — | Not stated | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is Facet 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 Facet?
Facet is made by Seaspine Orthopedics Corporation. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does Facet come in?
The FDA device database does not list sizes for Facet. Check the instructions for use or ask a Seaspine Orthopedics Corporation representative.
Is Facet MRI safe?
The FDA device database entry for Facet does not state its MRI safety status. Check the labeling before MRI.
Is Facet FDA cleared?
Facet is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Seaspine Orthopedics Corporation sales representative?
Seaspine Orthopedics Corporation has not listed representatives on LA Vascular yet. Visit the Seaspine Orthopedics Corporation 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.