FDA device listing
Sirius Femoral,Stem, Size 30A
FDA device listing 1660557033 · Zimmer Inc
Key facts
| Proprietary names | Sirius Femoral,Stem, Size 30A |
|---|---|
| Owner/operator | Zimmer Inc |
| Owner/operator number | 1825034 |
| Premarket submissions | K142295 |
| Product codes | JDG, JDI, KWL, KWY, KWZ, LPH, LZO, LZY, MEH, OQG, OQH, OQI and 1 more |
| Device names | JDG - Prosthesis, Hip, Femoral Component, Cemented, Metal, JDI - Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented, KWL - Prosthesis, Hip, Hemi-, Femoral, Metal, 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, LZO - Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented, LZY - Prosthesis, Hip, Hemi-, Femoral, Metal Ball, MEH - Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate, OQG - Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented, OQH - Hip, Semi-Constrained, Cemented, Metal/Polymer + Additive, Cemented, OQI - Hip, Semi-Constrained, Cemented, Metal/Ceramic/Polymer + Additive, Porous Uncemented and 1 more |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3310, 888.3350, 888.3353, 888.3358, 888.3360, 888.3390 |
| Review panels | Orthopedic |
| Registered establishments | BIOMET, INC. |
| Establishment registrations | 1825034 |
| FEI numbers | 1825034 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 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