Kyphoplasty systems

Modulift

by Aesculap Implant Systems, LLC

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.

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Modulift models and sizes

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

Model / catalog no.SizeMRIStatus
MF708Rβ€” Not statedAvailable
MF710Rβ€” Not statedAvailable
MF806Rβ€” Not statedAvailable
MF854Rβ€” Not statedAvailable
MF857Rβ€” Not statedAvailable

Procedures that use kyphoplasty systems

Frequently asked questions

What is Modulift 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 Modulift?

Modulift is made by Aesculap Implant Systems, LLC. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.

What sizes does Modulift come in?

The FDA device database does not list sizes for Modulift. Check the instructions for use or ask a Aesculap Implant Systems, LLC representative.

Is Modulift MRI safe?

The FDA device database entry for Modulift does not state its MRI safety status. Check the labeling before MRI.

Is Modulift FDA cleared?

Modulift is registered in the FDA's Global Unique Device Identification Database (GUDID).

How do I contact a Aesculap Implant Systems, LLC sales representative?

Aesculap Implant Systems, LLC has not listed representatives on LA Vascular yet. Visit the Aesculap Implant Systems, 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.

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