FDA product code IQQ: Joint, Shoulder, External Limb Component
IQQ is the FDA product code for joint, shoulder, external limb component. It is a Class I device, regulated under 21 CFR 890.3420 and reviewed by the Physical Medicine panel. Devices under IQQ reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Joint, Shoulder, External Limb Component |
| Device class | Class I |
| Regulation | 21 CFR 890.3420 |
| Review panel | PM — Physical Medicine |
| Medical specialty | Physical Medicine |
| Premarket route | 510(k) exempt |
| GMP exempt | Yes |
Recalls for IQQ devices
openFDA lists no recalls for product code IQQ.
Frequently asked questions
What is FDA product code IQQ?
IQQ is the FDA product code for joint, shoulder, external limb component. It is a Class I device, regulated under 21 CFR 890.3420 and reviewed by the Physical Medicine panel.
What device class is IQQ?
Class I, regulation 21 CFR 890.3420. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code IQQ
- Run a recall and safety report across every IQQ manufacturer
- Watch product code IQQ 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.
All Physical Medicine product codes · FDA product code lookup