FDA device listing
Neo Pedicle Screw System
FDA device listing 1914421205 · Neo Spine USA Inc.
Key facts
| Proprietary names | Neo Pedicle Screw System |
|---|---|
| Owner/operator | Neo Spine USA Inc. |
| Owner/operator number | 10056088 |
| Premarket submissions | K222256 |
| Product codes | NDN, NKB, PML |
| Device names | NDN - Cement, Bone, Vertebroplasty, NKB - Thoracolumbosacral Pedicle Screw System, PML - Bone Cement, Posterior Screw Augmentation |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3027, 888.3070 |
| Review panels | Orthopedic |
| Registered establishments | NEO SPINE USA INC. |
| Establishment registrations | 3014003062 |
| FEI numbers | 3014003062 |
| Establishment operations | Complaint File Establishment |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database