Joint Stim, Model 1000
by Pain Management Technologies 510(k)
Active
510(k) K073386
Overview
The Joint Stim, Model 1000 is a transcutaneous electrical stimulator designed for arthritis management. It delivers controlled electrical impulses to the joint, intended to modulate pain and improve function in affected areas. The device combines electrotherapy with compression to target symptoms associated with osteoarthritis and rheumatoid arthritis.
This device is supplied as a reusable system, consisting of a stimulation unit and conductive silver fabric electrode patches applied with a knee compression wrap. It is classified as a Class II medical device under FDA regulations and holds a 510(k) clearance (K073386). The device is intended for use in clinical or home settings, with no specific MRI safety restrictions noted. Storage and handling follow standard electrical medical device protocols.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK073386 | Date30 Jul 2008 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — FDA 510(k) Active
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- 510(k) Number
- FDA Product Code
- NYN
- Device Class
- Class II
- Regulation
- 21 CFR Part 882.5890
- Advisory Committee
- Neurology
- FDA Decision
- SESE Substantially Equivalent
Other devices from Pain Management Technologies
Questions
What is the Joint Stim Model 1000 used for?
The Joint Stim Model 1000 is designed to manage arthritis symptoms by delivering controlled electrical impulses to affected joints. It combines electrotherapy with compression to help modulate pain and improve function in areas impacted by osteoarthritis or rheumatoid arthritis. The device targets specific symptoms associated with these conditions, providing relief through targeted stimulation.
How is the Joint Stim Model 1000 supplied?
The Joint Stim Model 1000 is supplied as a reusable system, consisting of a stimulation unit and conductive silver fabric electrode patches. These patches are applied with a knee compression wrap, allowing the device to deliver both electrical impulses and compression therapy simultaneously. This setup ensures ease of use in clinical or home settings.
Is the Joint Stim Model 1000 single-use or reusable?
The Joint Stim Model 1000 is designed as a reusable device. The stimulation unit and electrode patches are intended for repeated use, provided they are handled and stored according to standard electrical medical device protocols. This makes it a cost-effective option for ongoing arthritis management.
What storage and handling guidelines should be followed?
The Joint Stim Model 1000 should be stored and handled following standard protocols for electrical medical devices. This includes keeping the device in a clean, dry environment, away from direct sunlight or extreme temperatures, and ensuring the electrode patches are stored properly to maintain their conductive properties. Proper storage ensures the device remains functional and safe for use.
Are there any MRI safety restrictions for the Joint Stim Model 1000?
No specific MRI safety restrictions are noted for the Joint Stim Model 1000. However, it is always recommended to consult the device’s instructions for use and any additional manufacturer guidelines before using it in proximity to MRI equipment. Standard precautions for electrical medical devices should also be observed.