Kyphoplasty systems
Kalitec Disc Prep
A hand-held manual surgical instrument designed to push a cartilage or bone graft into a position from which the graft can be delivered into a chondral defect [e.g., during anterior cruciate ligament (ACL) reconstruction surgery]. This device is available in a variety of designs, such as a plunger made of high-grade materials [e.g., stainless steel or titanium (Ti)] used to advance the graft down its tubular-shaped holder or possibly a bone graft funnel and into place; it is also available in a variety of sizes. This is a reusable device.
Where to buy Kalitec Disc Prep
We do not have contact details for Kalitec Direct LLC yet. Send a request and we will route it to the right person for your country.
Kalitec Disc Prep models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| 19-K01-6240 | — | Not stated | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is Kalitec Disc Prep used for?
A hand-held manual surgical instrument designed to push a cartilage or bone graft into a position from which the graft can be delivered into a chondral defect [e.g., during anterior cruciate ligament (ACL) reconstruction surgery]. This device is available in a variety of designs, such as a plunger made of high-grade materials [e.g., stainless steel or titanium (Ti)] used to advance the graft down its tubular-shaped holder or possibly a bone graft funnel and into place; it is also available in a variety of sizes. This is a reusable device.
Who makes Kalitec Disc Prep?
Kalitec Disc Prep is made by Kalitec Direct LLC. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does Kalitec Disc Prep come in?
The FDA device database does not list sizes for Kalitec Disc Prep. Check the instructions for use or ask a Kalitec Direct LLC representative.
Is Kalitec Disc Prep MRI safe?
The FDA device database entry for Kalitec Disc Prep does not state its MRI safety status. Check the labeling before MRI.
Is Kalitec Disc Prep FDA cleared?
Kalitec Disc Prep is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Kalitec Direct LLC sales representative?
Kalitec Direct LLC has not listed representatives on LA Vascular yet. Visit the Kalitec Direct 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.