FDA device listing
MDM Hip System Instrumentation,RAS System Instrumentation,Restoration Anatomic Shell,Stryker Orthopaedics…
FDA device listing 1245771922 · STRYKER CORP.
Key facts
| Proprietary names | MDM Hip System Instrumentation,RAS System Instrumentation,Restoration Anatomic Shell,Stryker Orthopaedics Instruments,Trident Hip System Instrumentation |
|---|---|
| Owner/operator | STRYKER CORP. |
| Owner/operator number | 1811755 |
| Premarket submissions | K151264 |
| Product codes | LPH |
| Device names | LPH - Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3358 |
| Review panels | Orthopedic |
| Registered establishments | HOWMEDICA OSTEONICS CORP, Stryker (Suzhou) Medical Technology Co.,Ltd. |
| Establishment registrations | 2249697, 3007913880 |
| FEI numbers | 3003070421, 3007913880 |
| Establishment operations | Contract Manufacturer, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None 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