Kyphoplasty systems

Citrefix Center Shaft Retaining Clamp

by Acuitive Technologies, Inc.

A hand-held manual surgical instrument designed for the surgical insertion and/or extraction of a non-tissue based (inorganic) orthopaedic implant (e.g., a bone nail, spiral blade, or bone fixation plate). It is an instrument in a one-piece or modular configuration with a region that will attach/fit/lock to part of the implant, and typically features either a mechanism to apply a striking force (e.g., on a pad/flange) a mechanism for twisting (screwing) (e.g., T-handle), or a plunger mechanism to deploy a guide to drive the implant into place. This is a reusable device.

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Citrefix Center Shaft Retaining Clamp models and sizes

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

Model / catalog no.SizeMRIStatus
40-100-0010— Not statedAvailable

Procedures that use kyphoplasty systems

Frequently asked questions

What is Citrefix Center Shaft Retaining Clamp used for?

A hand-held manual surgical instrument designed for the surgical insertion and/or extraction of a non-tissue based (inorganic) orthopaedic implant (e.g., a bone nail, spiral blade, or bone fixation plate). It is an instrument in a one-piece or modular configuration with a region that will attach/fit/lock to part of the implant, and typically features either a mechanism to apply a striking force (e.g., on a pad/flange) a mechanism for twisting (screwing) (e.g., T-handle), or a plunger mechanism to deploy a guide to drive the implant into place. This is a reusable device.

Who makes Citrefix Center Shaft Retaining Clamp?

Citrefix Center Shaft Retaining Clamp is made by Acuitive Technologies, Inc.. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.

What sizes does Citrefix Center Shaft Retaining Clamp come in?

The FDA device database does not list sizes for Citrefix Center Shaft Retaining Clamp. Check the instructions for use or ask a Acuitive Technologies, Inc. representative.

Is Citrefix Center Shaft Retaining Clamp MRI safe?

The FDA device database entry for Citrefix Center Shaft Retaining Clamp does not state its MRI safety status. Check the labeling before MRI.

Is Citrefix Center Shaft Retaining Clamp FDA cleared?

Citrefix Center Shaft Retaining Clamp is registered in the FDA's Global Unique Device Identification Database (GUDID).

How do I contact a Acuitive Technologies, Inc. sales representative?

Acuitive Technologies, Inc. has not listed representatives on LA Vascular yet. Visit the Acuitive Technologies, 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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