FDA device listing
aprevo Transforaminal Lumbar Interbody Fusion
FDA device listing 1530284282 · Boulder BioMed dba Boulder iQ
Key facts
| Proprietary names | aprevo Transforaminal Lumbar Interbody Fusion |
|---|---|
| Owner/operator | Boulder BioMed dba Boulder iQ |
| Owner/operator number | 10058905 |
| 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 | BOULDER BIOMED LLC |
| Establishment registrations | 3015151147 |
| FEI numbers | 3015151147 |
| Establishment operations | Contract Sterilizer |
| 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