Kyphoplasty systems

PCD, VertaPlex

by Stryker Corporation

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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Where to buy PCD, VertaPlex

Contact Stryker Corporation directly; they can quote, ship, or point you to the distributor for your country.

From stryker.com, checked October 2026.

No reply, or outside their markets? Send us a request and we route it to a rep or distributor for your country.

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PCD, VertaPlex models and sizes

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

Model / catalog no.SizeMRIStatus
0507486000Angle 90.0 ° Not statedAvailable
0507489000— Not statedAvailable
0507586000Angle 90.0 ° Not statedAvailable
0507589000— Not statedAvailable

Procedures that use kyphoplasty systems

Frequently asked questions

What is PCD, VertaPlex 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 PCD, VertaPlex?

PCD, VertaPlex is made by Stryker Corporation. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.

What sizes does PCD, VertaPlex come in?

Sizes listed for PCD, VertaPlex: Angle: 90 °. Confirm availability with the manufacturer's instructions for use.

Is PCD, VertaPlex MRI safe?

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

Is PCD, VertaPlex FDA cleared?

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

How do I contact a Stryker Corporation sales representative?

Stryker Corporation has not listed representatives on LA Vascular yet. Visit the Stryker Corporation 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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