FDA product code MLQ: Inhibitor, Peridural Fibrosis (Adhesion Barrier)
MLQ is the FDA product code for inhibitor, peridural fibrosis (adhesion barrier). It is a Class III device, reviewed by the Neurology panel. Devices under MLQ reach the market by PMA; FDA lists no cleared 510(k)s for it. 1 PMA application cites this product code.
Classification
| Field | Value |
|---|---|
| Device name | Inhibitor, Peridural Fibrosis (Adhesion Barrier) |
| Device class | Class III |
| Review panel | NE — Neurology |
| Medical specialty | Unknown |
| Premarket route | PMA |
Recalls for MLQ devices
openFDA lists no recalls for product code MLQ.
Frequently asked questions
What is FDA product code MLQ?
MLQ is the FDA product code for inhibitor, peridural fibrosis (adhesion barrier). It is a Class III device, reviewed by the Neurology panel.
What device class is MLQ?
Class III. Typical premarket route: PMA.
Next steps
- Run an FDA pathway report with predicate devices for product code MLQ
- Run a recall and safety report across every MLQ manufacturer
- Watch product code MLQ 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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