FDA product code PZT: Peripheral Blood Processing Device For Osteoarthritis
PZT is the FDA product code for peripheral blood processing device for osteoarthritis. It is a Not classified device, reviewed by the Hematology panel. Devices under PZT reach the market by Contact FDA; FDA lists no cleared 510(k)s for it.
Definition
Preparation of autologous anti-inflammatory (AAI) solution from a small sample of peripheral blood for treatment of osteoarthritis.
Classification
| Field | Value |
|---|---|
| Device name | Peripheral Blood Processing Device For Osteoarthritis |
| Device class | Not classified |
| Review panel | HE — Hematology |
| Medical specialty | Unknown |
| Premarket route | Contact FDA |
Recalls for PZT devices
openFDA lists no recalls for product code PZT.
Frequently asked questions
What is FDA product code PZT?
PZT is the FDA product code for peripheral blood processing device for osteoarthritis. It is a Not classified device, reviewed by the Hematology panel.
What device class is PZT?
Not classified. Typical premarket route: Contact FDA.
Next steps
- Run an FDA pathway report with predicate devices for product code PZT
- Run a recall and safety report across every PZT manufacturer
- Watch product code PZT 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.