FDA device listing
Modulus femoral stems; Modular heads; Lock Bipolar heads; Cemented cups
FDA device listing 1862422110 · WESTLAKE PLASTICS EUROPE
Key facts
| Proprietary names | Modulus femoral stems; Modular heads; Lock Bipolar heads; Cemented cups |
|---|---|
| Owner/operator | WESTLAKE PLASTICS EUROPE |
| Owner/operator number | 10048274 |
| Product codes | JDI, KWY, KWZ, LPH |
| Device names | JDI - Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented, KWY - Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented, KWZ - Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer, LPH - Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3310, 888.3350, 888.3358, 888.3390 |
| Review panels | Orthopedic |
| Registered establishments | WESTLAKE PLASTICS EUROPE |
| Establishment registrations | 3011274144 |
| FEI numbers | 3011274144 |
| 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