FDA device listing
LDR SPINE EASYSPINE POSTERIOR OSTEOSYNTHESIS SYSTEM
FDA device listing 1100859899 · ZIMMER GMBH
Key facts
| Proprietary names | LDR SPINE EASYSPINE POSTERIOR OSTEOSYNTHESIS SYSTEM |
|---|---|
| Owner/operator | ZIMMER GMBH |
| Owner/operator number | 9064978 |
| Premarket submissions | K070341 |
| Product codes | KWP, MNH, MNI, NKB |
| Device names | KWP - Appliance, Fixation, Spinal Interlaminal, MNH - Orthosis, Spondylolisthesis Spinal Fixation, MNI - Orthosis, Spinal Pedicle Fixation, NKB - Thoracolumbosacral Pedicle Screw System |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3050, 888.3070 |
| Review panels | Orthopedic |
| Registered establishments | Biomet Global Supply Chain Center B.V. |
| Establishment registrations | 3013055499 |
| FEI numbers | 3013055499 |
| Establishment operations | Foreign Exporter |
| 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