# K162702: Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table

- Pathway: 510(k) (Traditional)
- Applicant: Stl International, Inc.
- Decided: Dec 30, 2016 after 93 days
- Product code: HST (Apparatus, Traction, Non-Powered)
- Device class: 1
- Regulation: 21 CFR 888.5850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K110858 (2011). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K110858: LO-Bak Trax, Roland F Berthiaume, DC (2011) Summary page 4.

## Indications for use
Teeter Decompression Devices are multiple user, reusable devices for home use, intended to provide traction to the spine while stretching the para-spinal muscles and soft tissues. The devices provide non-powered traction and are meant for use by adults. Use of the Teeter Decompression Devices is indicated for the following conditions: back pain, muscle tension, degenerative disc disease, spinal degenerative joint disease, spinal stenosis, herniated disc, spinal curvature due to tight muscles, sciatica, muscle spasm, and facet syndrome.

Source page: https://510kreport.com/device/K162702
Methodology: https://510kreport.com/methodology