# K121702: Orthocor Active Device Orthocor General Use Active Device

- Pathway: 510(k) (Traditional)
- Applicant: Orthocor Medical
- Decided: May 6, 2013 after 332 days
- Product code: ILX (Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat)
- Device class: 2
- Regulation: 21 CFR 890.5290
- 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 K903675 (1991). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K091996: Orthocor Knee System Basic, Orthocor Medical (2009) Summary page 5.

## Most influential descendants
- K241395: Active System; Avenue8 (2024), 0 descendants of its own

## Indications for use
The device is indicated for adjunctive use in the palliative treatment of postoperative pain and edema in superficial soft tissue.

Source page: https://510kreport.com/device/K121702
Methodology: https://510kreport.com/methodology