FDA device listing
V-Steady Cement
FDA device listing 1404023010 · ULRICH MEDICAL USA, INC.
Key facts
| Proprietary names | V-Steady Cement |
|---|---|
| Owner/operator | ULRICH MEDICAL USA, INC. |
| Owner/operator number | 9062154 |
| Premarket submissions | K231809 |
| Product codes | NKB, PML |
| Device names | 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 | ULRICH MEDICAL USA, INC. |
| Establishment registrations | 3005823819 |
| FEI numbers | 3005532635 |
| Establishment operations | Complaint File Establishment |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None 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