FDA device listing
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA device listing 1649132437 · Culver Tool & Engineering LLC dba SpiTrex CTE
Key facts
| Owner/operator | Culver Tool & Engineering LLC dba SpiTrex CTE |
|---|---|
| Owner/operator number | 10043008 |
| Product codes | MAX |
| Device names | MAX - Intervertebral Fusion Device With Bone Graft, Lumbar |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3080 |
| Review panels | Orthopedic |
| Registered establishments | CULVER TOOL & ENGINEERING |
| Establishment registrations | 3010047454 |
| FEI numbers | 3010047454 |
| Establishment operations | Contract Manufacturer |
| 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