FDA product code QHP: Vertebral Body Tethering System
QHP is the FDA product code for vertebral body tethering system. It is a Not classified device, reviewed by the Orthopedic panel. Devices under QHP reach the market by Unclassified; FDA lists no cleared 510(k)s for it.
Definition
Anterior-based stabilization or correction of juvenile or adolescent idiopathic scoliosis without the use of fusion
Classification
| Field | Value |
|---|---|
| Device name | Vertebral Body Tethering System |
| Device class | Not classified |
| Review panel | OR — Orthopedic |
| Medical specialty | Unknown |
| Premarket route | Unclassified |
| Implant | Yes |
Recalls for QHP devices
openFDA lists no recalls for product code QHP.
Frequently asked questions
What is FDA product code QHP?
QHP is the FDA product code for vertebral body tethering system. It is a Not classified device, reviewed by the Orthopedic panel.
What device class is QHP?
Not classified. Typical premarket route: Unclassified.
Next steps
- Run an FDA pathway report with predicate devices for product code QHP
- Run a recall and safety report across every QHP manufacturer
- Watch product code QHP 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.