FDA device listing
Zimmer NexGen Tibial and Femoral Augments
FDA device listing 1665581299 · Zimmer Biomet APAC DFE
Key facts
| Proprietary names | Zimmer NexGen Tibial and Femoral Augments |
|---|---|
| Owner/operator | Zimmer Biomet APAC DFE |
| Owner/operator number | 10056128 |
| Premarket submissions | K152494 |
| Product codes | JWH, KRO |
| Device names | JWH - Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer, KRO - Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3510, 888.3560 |
| Review panels | Orthopedic |
| Registered establishments | Zimmer Biomet Korea Ltd., Zimmer Biomet Taiwan Co., Ltd., Zimmer (Shanghai) Medical International Trading Co., Ltd. |
| Establishment registrations | 3011683674, 3015207155, 3015542154 |
| FEI numbers | 3011683674, 3015207155, 3015542154 |
| Establishment operations | Foreign Exporter |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 100–999 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