FDA device listing
XPS Nexus System, XPS Nexus Foot Control, XPS Nexus IV Pole
FDA device listing 1388736099 · Medtronic, Inc.
Key facts
| Proprietary names | XPS Nexus System, XPS Nexus Foot Control, XPS Nexus IV Pole |
|---|---|
| Owner/operator | Medtronic, Inc. |
| Owner/operator number | 2112641 |
| Premarket submissions | K150728 |
| Product codes | ERL |
| Device names | ERL - Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece |
| Device class | Class II |
| Classification regulations (21 CFR) | 874.4250 |
| Review panels | Ear, Nose, & Throat |
| Registered establishments | Medtronic Engineering and Innovation Center (MEIC), MEDTRONIC XOMED, INC. |
| Establishment registrations | 1045254, 3018094310 |
| FEI numbers | 1045254, 3018094310 |
| Establishment operations | Complaint File Establishment, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 10–99 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