FDA device listing
Osteosynthesis Plate System
FDA device listing 1183950042 · Signature Orthopaedics Pty Limited
Key facts
| Proprietary names | Osteosynthesis Plate System |
|---|---|
| Owner/operator | Signature Orthopaedics Pty Limited |
| Owner/operator number | 10037793 |
| Premarket submissions | K241599 |
| Product codes | HRS, HTN, HWC |
| Device names | HRS - Plate, Fixation, Bone, HTN - Washer, Bolt Nut, HWC - Screw, Fixation, Bone |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3030, 888.3040 |
| Review panels | Orthopedic |
| Registered establishments | Signature Orthopaedics Europe Ltd, SIGNATURE ORTHOPAEDICS PTY LIMITED |
| Establishment registrations | 3008262872, 3014763043 |
| FEI numbers | 3008262872, 3014763043 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 100–999 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