Kyphoplasty systems
SPARK - Instruments
by WALDEMAR LINK GmbH & Co. KG
A hand-held manual surgical instrument designed to impart force to an orthopaedic implantable device that is inserted to fix or fasten together bones. The device is frequently used to insert devices such as screws, nails, plates, or wires that are used to fix fractured or damaged bones and/or to attach orthopaedic prostheses to the bones. It is typically made of high-grade stainless steel or titanium (Ti). This is a reusable device.
Where to buy SPARK - Instruments
We do not have contact details for WALDEMAR LINK GmbH & Co. KG yet. Send a request and we will route it to the right person for your country.
SPARK - Instruments 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 |
|---|---|---|---|
| 445-210/00 | — | Not stated | Available |
| 445-309/00 | — | Not stated | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is SPARK - Instruments used for?
A hand-held manual surgical instrument designed to impart force to an orthopaedic implantable device that is inserted to fix or fasten together bones. The device is frequently used to insert devices such as screws, nails, plates, or wires that are used to fix fractured or damaged bones and/or to attach orthopaedic prostheses to the bones. It is typically made of high-grade stainless steel or titanium (Ti). This is a reusable device.
Who makes SPARK - Instruments?
SPARK - Instruments is made by WALDEMAR LINK GmbH & Co. KG. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does SPARK - Instruments come in?
The FDA device database does not list sizes for SPARK - Instruments. Check the instructions for use or ask a WALDEMAR LINK GmbH & Co. KG representative.
Is SPARK - Instruments MRI safe?
The FDA device database entry for SPARK - Instruments does not state its MRI safety status. Check the labeling before MRI.
Is SPARK - Instruments FDA cleared?
SPARK - Instruments is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a WALDEMAR LINK GmbH & Co. KG sales representative?
WALDEMAR LINK GmbH & Co. KG has not listed representatives on LA Vascular yet. Visit the WALDEMAR LINK GmbH & Co. KG 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.