FDA device listing
SPINEVISION LUMIS CANNULATED POLYAXIAL PEDICLE SCREW FIXATION SYSTEM
FDA device listing 1997801806 · Safe Medical
Key facts
| Proprietary names | SPINEVISION LUMIS CANNULATED POLYAXIAL PEDICLE SCREW FIXATION SYSTEM |
|---|---|
| Owner/operator | Safe Medical |
| Owner/operator number | 10054418 |
| Product codes | KWP, KWQ, MNH, MNI |
| Device names | KWP - Appliance, Fixation, Spinal Interlaminal, KWQ - Appliance, Fixation, Spinal Intervertebral Body, MNH - Orthosis, Spondylolisthesis Spinal Fixation, MNI - Orthosis, Spinal Pedicle Fixation |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3050, 888.3060, 888.3070 |
| Review panels | Orthopedic |
| Registered establishments | Safe Medical |
| Establishment registrations | 3013548554 |
| FEI numbers | 3013548554 |
| 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