Kyphoplasty systems

Sacroiliac Joint Fusion System

by Xtant Medical Holdings, Inc.

A collection of surgical instruments and devices intended to be used for the implantation of a sacroiliac joint transarticular fixation/arthrodesis implant during a minimally-invasive procedure. It typically consists of a tray, dedicated soft-tissue protectors, depth gauges, pin sleeves, drill sleeves, drill bits, broaches, a parallel pin guide, handles, slide hammer shafts, impactors, and a removal/adaptor tool; the implant(s) is not included. This is a reusable device.

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Sacroiliac Joint Fusion System models and sizes

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

Model / catalog no.SizeMRIStatus
C079-0042— Not statedAvailable

Procedures that use kyphoplasty systems

Frequently asked questions

What is Sacroiliac Joint Fusion System used for?

A collection of surgical instruments and devices intended to be used for the implantation of a sacroiliac joint transarticular fixation/arthrodesis implant during a minimally-invasive procedure. It typically consists of a tray, dedicated soft-tissue protectors, depth gauges, pin sleeves, drill sleeves, drill bits, broaches, a parallel pin guide, handles, slide hammer shafts, impactors, and a removal/adaptor tool; the implant(s) is not included. This is a reusable device.

Who makes Sacroiliac Joint Fusion System?

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

What sizes does Sacroiliac Joint Fusion System come in?

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

Is Sacroiliac Joint Fusion System MRI safe?

The FDA device database entry for Sacroiliac Joint Fusion System does not state its MRI safety status. Check the labeling before MRI.

Is Sacroiliac Joint Fusion System FDA cleared?

Sacroiliac Joint Fusion System 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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