FDA device listing
Summit SI OCT Spinal Fixation System
FDA device listing 1333015038 · SYNTHES GMBH / Synthes Produktions GmbH
Key facts
| Proprietary names | Summit SI OCT Spinal Fixation System |
|---|---|
| Owner/operator | SYNTHES GMBH / Synthes Produktions GmbH |
| Owner/operator number | 9071542 |
| Premarket submissions | K151885 |
| Product codes | KWP, NKG |
| Device names | KWP - Appliance, Fixation, Spinal Interlaminal, NKG - Posterior Cervical Screw System |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3050, 888.3075 |
| Review panels | Orthopedic |
| Registered establishments | Synthes GMBH, SYNTHES GMBH |
| Establishment registrations | 3000270450, 3009417901 |
| FEI numbers | 3000270450, 3009417901 |
| Establishment operations | Manufacturer, Specification Developer |
| 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