FDA product code NCO: Implant, Cartilage, For Articular Cartilage Repair
NCO is the FDA product code for implant, cartilage, for articular cartilage repair. It is a Class III device, reviewed by the Orthopedic panel. Devices under NCO reach the market by Contact FDA; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Implant, Cartilage, For Articular Cartilage Repair |
| Device class | Class III |
| Review panel | OR — Orthopedic |
| Medical specialty | Unknown |
| Premarket route | Contact FDA |
| Implant | Yes |
Recalls for NCO devices
openFDA lists no recalls for product code NCO.
Frequently asked questions
What is FDA product code NCO?
NCO is the FDA product code for implant, cartilage, for articular cartilage repair. It is a Class III device, reviewed by the Orthopedic panel.
What device class is NCO?
Class III. Typical premarket route: Contact FDA.
Next steps
- Run an FDA pathway report with predicate devices for product code NCO
- Run a recall and safety report across every NCO manufacturer
- Watch product code NCO 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 Orthopedic product codes · FDA product code lookup · 510(k) database search · 510(k) review times