Kyphoplasty systems
Cross-Fuse II PEEK IBF System
A collection of instruments and devices intended to be used for the placement of an internal orthopaedic fixation system into or onto all types of bones (e.g., bones of limbs, spine, pelvis, or craniomaxillofacial). It is a non-dedicated device that includes various metallic and/or plastic reusable devices [e.g., retractors, rods, clamps, drills, pins, saws, screwdrivers, guides, trials, impactors] intended to be used for the implantation of any type of internal orthopaedic fixation system; the implant(s) is not included. This is a reusable device.
Where to buy Cross-Fuse II PEEK IBF System
We do not have contact details for Rti Surgical, Inc. yet. Send a request and we will route it to the right person for your country.
Cross-Fuse II PEEK IBF System 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 |
|---|---|---|---|
| 723-476 | — | Not stated | Available |
| 723-477 | — | Not stated | Available |
| 723-478 | — | Not stated | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is Cross-Fuse II PEEK IBF System used for?
A collection of instruments and devices intended to be used for the placement of an internal orthopaedic fixation system into or onto all types of bones (e.g., bones of limbs, spine, pelvis, or craniomaxillofacial). It is a non-dedicated device that includes various metallic and/or plastic reusable devices [e.g., retractors, rods, clamps, drills, pins, saws, screwdrivers, guides, trials, impactors] intended to be used for the implantation of any type of internal orthopaedic fixation system; the implant(s) is not included. This is a reusable device.
Who makes Cross-Fuse II PEEK IBF System?
Cross-Fuse II PEEK IBF System is made by Rti Surgical, Inc.. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does Cross-Fuse II PEEK IBF System come in?
The FDA device database does not list sizes for Cross-Fuse II PEEK IBF System. Check the instructions for use or ask a Rti Surgical, Inc. representative.
Is Cross-Fuse II PEEK IBF System MRI safe?
The FDA device database entry for Cross-Fuse II PEEK IBF System does not state its MRI safety status. Check the labeling before MRI.
Is Cross-Fuse II PEEK IBF System FDA cleared?
Cross-Fuse II PEEK IBF System is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Rti Surgical, Inc. sales representative?
Rti Surgical, Inc. has not listed representatives on LA Vascular yet. Visit the Rti Surgical, 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.