Kyphoplasty systems
META+ System MV
by Teknimed
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.
Where to buy META+ System MV
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META+ System MV 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 |
|---|---|---|---|
| T040352MV | — | Not stated | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is META+ System MV 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 META+ System MV?
META+ System MV is made by Teknimed. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does META+ System MV come in?
The FDA device database does not list sizes for META+ System MV. Check the instructions for use or ask a Teknimed representative.
Is META+ System MV MRI safe?
The FDA device database entry for META+ System MV does not state its MRI safety status. Check the labeling before MRI.
Is META+ System MV FDA cleared?
META+ System MV is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Teknimed sales representative?
Teknimed has not listed representatives on LA Vascular yet. Visit the Teknimed 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.