# K073386: Joint Stim, Model 1000

- Pathway: 510(k) (Traditional)
- Applicant: Pain Management Technologies
- Decided: Jul 30, 2008 after 240 days
- Product code: NYN (Stimulator, Electrical, Transcutaneous, For Arthritis)
- Device class: 2
- Regulation: 21 CFR 882.5890
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K971437 (1997). 4 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K030332: Modification to Bionicare Stimulator System, Model Bio-1000, Bionicare Medical Technologies, Inc. (2003) Summary page 1.
- K052625: Bionicare Stimulator System, Model Bio-1000, Bionicare Medical Technologies, Inc. (2005) Summary page 1.

## Most influential descendants
- K111557: X-Force (2011), 0 descendants of its own

## Indications for use
The J-Sirn I 000 'TM ' external, nonrinvaisive,. non-narcotic, electrotherapy system is indicated for use as an adjamnctive therapy in reducing the level of pain and symptoms associated with osteoarahritis of the knee and for overall improvement of the knee. The i-Stim I000 TM is also indicated -for use as an adjunctive therapy in reducing the level of pain, and _tiffness associated with pain, friom rheumatoid arthritis of the hand. These devices are to be used or sold only under the direct supervision or order of a licensed practitioner. A prescription is required to ohtain this product, The product can be used in the home or clinic by all patients in need.

Source page: https://510kreport.com/device/K073386
Methodology: https://510kreport.com/methodology