Kyphoplasty systems
Arcadius Xp C
by Aesculap AG
A hand-held surgical instrument intended to be used during implantation of an orthopaedic prosthesis, either manually or as a computer-assisted surgery (CAS) device, to aid in the navigation/placement of the prosthesis or other instruments [e.g., drill sleeves and guide wires (Kirschner wires), patella saw guide]. It may be used for the following applications: 1) to hold/align/fix/guide other instruments, prostheses, or prosthesis components; 2) to provide relative position landmarks; 3) to ascertain correct spatial orientation or limb alignment; and/or 4) as an interface (non-adaptive) between prosthesis components. This is a reusable device intended to be sterilized prior to use.
Where to buy Arcadius Xp C
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Arcadius Xp C 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 |
|---|---|---|---|
| ME073R | — | Not stated | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is Arcadius Xp C used for?
A hand-held surgical instrument intended to be used during implantation of an orthopaedic prosthesis, either manually or as a computer-assisted surgery (CAS) device, to aid in the navigation/placement of the prosthesis or other instruments [e.g., drill sleeves and guide wires (Kirschner wires), patella saw guide]. It may be used for the following applications: 1) to hold/align/fix/guide other instruments, prostheses, or prosthesis components; 2) to provide relative position landmarks; 3) to ascertain correct spatial orientation or limb alignment; and/or 4) as an interface (non-adaptive) between prosthesis components. This is a reusable device intended to be sterilized prior to use.
Who makes Arcadius Xp C?
Arcadius Xp C is made by Aesculap AG. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does Arcadius Xp C come in?
The FDA device database does not list sizes for Arcadius Xp C. Check the instructions for use or ask a Aesculap AG representative.
Is Arcadius Xp C MRI safe?
The FDA device database entry for Arcadius Xp C does not state its MRI safety status. Check the labeling before MRI.
Is Arcadius Xp C FDA cleared?
Arcadius Xp C is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Aesculap AG sales representative?
Aesculap AG has not listed representatives on LA Vascular yet. Visit the Aesculap AG 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.