Duns Number:056903080
Device Description: The InterX Electrode Accessories are a critical part of the InterX non-invasive interactiv The InterX Electrode Accessories are a critical part of the InterX non-invasive interactive neurostimulation (NIN) system. The InterX Personal Flexible Array can be connected to both the InterX 1000 and InterX 5002 Devices via this Y-Cable. The InterX Personal Flexible Array is intended for single patient use. Both the InterX 1000 and InterX 5002 devices are designed to provide 10 minutes of treatment options and can be used unattended once treatment parameters have been set on either the InterX 1000 or InterX 5002 device or dynamically for muscle re-education. This Y-Cable along with the InterX Personal Flexible Array is indicated for symptomatic relief and management of chronic intractable pain and also adjunctive treatment in the management of post-surgical and post traumatic pain.
Catalog Number
1589-001
Brand Name
InterX
Version/Model Number
1589
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
-
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
GXY
Product Code Name
Electrode, Cutaneous
Public Device Record Key
c8aa4e81-c34e-4fdf-aff3-870905f18f88
Public Version Date
February 19, 2021
Public Version Number
3
DI Record Publish Date
June 01, 2020
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 2 | A medical device with a moderate to high risk that requires special controls. | 16 |