FDA product code PCQ: Inhibitor, Postoperative Fibrosis (Spine Adhesion Barrier)
PCQ is the FDA product code for inhibitor, postoperative fibrosis (spine adhesion barrier). It is a Not classified device, reviewed by the Neurology panel. Devices under PCQ reach the market by Contact FDA; FDA lists no cleared 510(k)s for it.
Definition
Intended for use as a mechanical barrier to adhesion formation.
Classification
| Field | Value |
|---|---|
| Device name | Inhibitor, Postoperative Fibrosis (Spine Adhesion Barrier) |
| Device class | Not classified |
| Review panel | NE — Neurology |
| Medical specialty | Unknown |
| Premarket route | Contact FDA |
Recalls for PCQ devices
openFDA lists no recalls for product code PCQ.
Frequently asked questions
What is FDA product code PCQ?
PCQ is the FDA product code for inhibitor, postoperative fibrosis (spine adhesion barrier). It is a Not classified device, reviewed by the Neurology panel.
What device class is PCQ?
Not classified. Typical premarket route: Contact FDA.
Next steps
- Run an FDA pathway report with predicate devices for product code PCQ
- Run a recall and safety report across every PCQ manufacturer
- Watch product code PCQ 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.