Kyphoplasty systems

Osseoflex PC Pre-Curved Bone Tamp 10ga

by Osseon LLC

A collection of sterile manual devices intended to create a percutaneous access channel within a vertebral body or other bones (e.g., hand, radius, tibia, calcaneus) prior to the use of an inflatable balloon (e.g., a balloon catheter or balloon tamp) to create a bone space during kyphoplasty/osteoplasty. It typically consists of bone access needles/cannulae, orthopaedic bone wires (Kirschner wires), a drill, and a curette. It is used in orthopaedic surgery, typically under fluoroscopic guidance, to treat a patient diagnosed with compression fractures. This is a single-use device.

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Osseoflex PC Pre-Curved Bone Tamp 10ga models and sizes

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

Model / catalog no.SizeMRIStatus
PC-0270Needle Gauge 10 G Not statedAvailable

Procedures that use kyphoplasty systems

Frequently asked questions

What is Osseoflex PC Pre-Curved Bone Tamp 10ga used for?

A collection of sterile manual devices intended to create a percutaneous access channel within a vertebral body or other bones (e.g., hand, radius, tibia, calcaneus) prior to the use of an inflatable balloon (e.g., a balloon catheter or balloon tamp) to create a bone space during kyphoplasty/osteoplasty. It typically consists of bone access needles/cannulae, orthopaedic bone wires (Kirschner wires), a drill, and a curette. It is used in orthopaedic surgery, typically under fluoroscopic guidance, to treat a patient diagnosed with compression fractures. This is a single-use device.

Who makes Osseoflex PC Pre-Curved Bone Tamp 10ga?

Osseoflex PC Pre-Curved Bone Tamp 10ga is made by Osseon LLC. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.

What sizes does Osseoflex PC Pre-Curved Bone Tamp 10ga come in?

Sizes listed for Osseoflex PC Pre-Curved Bone Tamp 10ga: Needle Gauge: 10 G. Confirm availability with the manufacturer's instructions for use.

Is Osseoflex PC Pre-Curved Bone Tamp 10ga MRI safe?

The FDA device database entry for Osseoflex PC Pre-Curved Bone Tamp 10ga does not state its MRI safety status. Check the labeling before MRI.

Is Osseoflex PC Pre-Curved Bone Tamp 10ga FDA cleared?

Osseoflex PC Pre-Curved Bone Tamp 10ga is registered in the FDA's Global Unique Device Identification Database (GUDID).

How do I contact a Osseon LLC sales representative?

Osseon LLC has not listed representatives on LA Vascular yet. Visit the Osseon 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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