FDA device listing
G7 ACETABULAR SYSTEM
FDA device listing 1049086341 · Micropulse
Key facts
| Proprietary names | G7 ACETABULAR SYSTEM |
|---|---|
| Owner/operator | Micropulse |
| Owner/operator number | 10042100 |
| Product codes | JDI, KWZ, LPH, LZO, OQG, OQH, OQI, PBI |
| Device names | JDI - Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented, 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, 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, PBI - Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer, + Additive |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3310, 888.3350, 888.3353, 888.3358 |
| Review panels | Orthopedic |
| Registered establishments | MICROPULSE INC |
| Establishment registrations | 1834379 |
| FEI numbers | 1000306303 |
| 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