FDA device listing
LimaCorpSPA9283 (CC) - CMD 24-1137 ProMade Hip,LimaCorpSPA9283 (CC) - CMD 24-1278 ProMade Hip,LimaCorpSPA9283 (CC) - CMD…
FDA device listing 1159684788 · STERIS Corporation
Key facts
| Proprietary names | LimaCorpSPA9283 (CC) - CMD 24-1137 ProMade Hip,LimaCorpSPA9283 (CC) - CMD 24-1278 ProMade Hip,LimaCorpSPA9283 (CC) - CMD 24-1298 ProMade Hip,LimaCorpSPA9283 (CC) - CMD 24-1336 ProMade Hip,LimaCorpSPA9283 (CC) - CMD 24-1396 ProMade Hip,LimaCorpSPA9283 (CC) - CMD 24-1417 ProMade Hip,LimaCorpSPA9283 (CC) - CMD 24-1434 ProMade Hip,LimaCorpSPA9283 (CC) - CMD 24-1439 Promade Hip,LimaCorpSPA9283 (CC)… |
|---|---|
| Owner/operator | STERIS Corporation |
| Owner/operator number | 10042227 |
| Product codes | KWA |
| Device names | KWA - Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component) |
| Device class | Class III |
| Classification regulations (21 CFR) | 888.3330 |
| Review panels | Orthopedic |
| Registered establishments | STERIS SPA |
| Establishment registrations | 3002806603 |
| FEI numbers | 3002806603 |
| Establishment operations | Contract Sterilizer |
| 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