Kyphoplasty systems

NuVasive Maximum Viscosity Spinal Cement System

by Teknimed

A collection of sterile surgical instruments, tools, and materials designed to prepare and apply bone cement during an orthopaedic surgical procedure (e.g., hip replacement, arthroplasty, or vertebroplasty). It typically includes items such as forceps, a mallet, cement delivery injectors, delivery tubes, and mixing devices; it may or may not include bone cement. This is a single-use device.

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NuVasive Maximum Viscosity Spinal Cement System models and sizes

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

Model / catalog no.SizeMRIStatus
NuVasive Max. Visco. Cem. System— MR SafeAvailable

Procedures that use kyphoplasty systems

Frequently asked questions

What is NuVasive Maximum Viscosity Spinal Cement System used for?

A collection of sterile surgical instruments, tools, and materials designed to prepare and apply bone cement during an orthopaedic surgical procedure (e.g., hip replacement, arthroplasty, or vertebroplasty). It typically includes items such as forceps, a mallet, cement delivery injectors, delivery tubes, and mixing devices; it may or may not include bone cement. This is a single-use device.

Who makes NuVasive Maximum Viscosity Spinal Cement System?

NuVasive Maximum Viscosity Spinal Cement System is made by Teknimed. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.

What sizes does NuVasive Maximum Viscosity Spinal Cement System come in?

The FDA device database does not list sizes for NuVasive Maximum Viscosity Spinal Cement System. Check the instructions for use or ask a Teknimed representative.

Is NuVasive Maximum Viscosity Spinal Cement System MRI safe?

The FDA device database lists NuVasive Maximum Viscosity Spinal Cement System as MR Safe. Always follow the specific MRI conditions in the labeling.

Is NuVasive Maximum Viscosity Spinal Cement System FDA cleared?

NuVasive Maximum Viscosity Spinal Cement System is registered in the FDA's Global Unique Device Identification Database (GUDID).

How do I contact a Teknimed sales representative?

Teknimed has not listed representatives on LA Vascular yet. Visit the Teknimed 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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