OZJ
- Product code
- OZJ
- Device name
- Inhibitor, Postoperative Fibrosis (Adhesion Barrier)
- Device class
- Class N
- Medical specialty
- Unknown
- Marketing pathway
- Contact ODE
FDA classification definition
The device is designed to coat surfaces exposed in tendon and peripheral nerve surgery, in order to form a temporary mechanical barrier that separates tissues for the purpose of reducing fibrosis and reducing the formation of adhesions.
Official FDA classification page: OZJ
Classification and pathway per current FDA publications. Data from openFDA (CC0).