# K150695: Modpod

- Pathway: 510(k) (Traditional)
- Applicant: Hollywog, LLC
- Decided: Aug 13, 2015 after 148 days
- Product code: ITH (Equipment, Traction, Powered)
- Device class: 2
- Regulation: 21 CFR 890.5900
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K894435 (1989). 20 ancestors in all.
No later device cites it as a predicate yet.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K051938: Triton/Tru-Trac/TX Traction Devices, Chattanooga Group (2005) Summary page 5.
- K053223: Triton/Tru-Trac/TX/Triton DTS Traction, Chattanooga Group (2006) Summary page 5.

## Indications for use
Modpod cervical traction provides mobilization of skeletal structures and muscles in static, intermittent, progressive, and regressive distraction forces to relieve pressures that may be causing pain of skeletal or muscular origin. These effects are achieved through decompression of intervertebral discs, that is, unloading due to distraction and positioning, and may be used to relieve peripheral radiation/sciatica and pain associated with: •Protruding discs •Bulging discs •Herniated discs •Degenerative disc disease •Posterior facet syndrome •Acute facet problems •Radicular pain •Prolapsed discs •Spinal root impingement •Hypomobility •Degenerative joint disease •Facet syndrome •Compressions fracture •Joint pain • Discogenic pain

Source page: https://510kreport.com/device/K150695
Methodology: https://510kreport.com/methodology