# K110858: LO-Bak Trax

- Pathway: 510(k) (Traditional)
- Applicant: Roland F Berthiaume, DC
- Decided: Aug 2, 2011 after 127 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Teeter Hang Up's Inversion Table, Model #tEP550: named in the summary without a submission number

## Most influential descendants
- K162702: Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table (2016), 0 descendants of its own

## Indications for use
Lo-Bak TRAX is intended for single person use by adults to provide portable, non-powered traction force to the lumbar spine and to stretch and relax the para-spinal muscles and soft tissues. Use of Lo-Bak TRAX is indicated for the following conditions: low back pain, degenerative disc disease, spinal degenerative joint disease, spinal stenosis, herniated disc, spinal curvature due to tight muscles, sciatica and muscle spasm.

Source page: https://510kreport.com/device/K110858
Methodology: https://510kreport.com/methodology