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