FDA device listing
AVS ANCHOR-C CERVICAL CAGE SYSTEM
FDA device listing 1279277642 · Classic Wire Cut Company, Inc.
Key facts
| Proprietary names | AVS ANCHOR-C CERVICAL CAGE SYSTEM |
|---|---|
| Owner/operator | Classic Wire Cut Company, Inc. |
| Owner/operator number | 9039170 |
| Product codes | OVE |
| Device names | OVE - Intervertebral Fusion Device With Integrated Fixation, Cervical |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3080 |
| Review panels | Orthopedic |
| Registered establishments | CLASSIC WIRE CUT COMPANY, INC. |
| Establishment registrations | 2031917 |
| FEI numbers | 3002929183 |
| Establishment operations | Contract Manufacturer, U.S. Manufacturer of Export Only Devices |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed 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