FDA product code MQO: Prosthetic Disc Nucleus Device
MQO is the FDA product code for prosthetic disc nucleus device. It is a Not classified device, reviewed by the Orthopedic panel. Devices under MQO reach the market by Contact FDA; FDA lists no cleared 510(k)s for it.
Definition
Export only
Classification
| Field | Value |
|---|---|
| Device name | Prosthetic Disc Nucleus Device |
| Device class | Not classified |
| Review panel | OR — Orthopedic |
| Medical specialty | Unknown |
| Premarket route | Contact FDA |
| Implant | Yes |
Recalls for MQO devices
openFDA lists no recalls for product code MQO.
Frequently asked questions
What is FDA product code MQO?
MQO is the FDA product code for prosthetic disc nucleus device. It is a Not classified device, reviewed by the Orthopedic panel.
What device class is MQO?
Not classified. Typical premarket route: Contact FDA.
Next steps
- Run an FDA pathway report with predicate devices for product code MQO
- Run a recall and safety report across every MQO manufacturer
- Watch product code MQO for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.