510(k) · Cleared
ClearedBack-on-Trac, Model 101BOT
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Back-On-Track, Inc. · HST Apparatus, Traction, Non-Powered
Cleared on Mar 15, 1999 after a 112-day review. FDA’s file for it is a 510(k) statement, which names no predicate.
- Decided
- Mar 15, 1999
- Review
- 112 days
- Class
- Class I
- Product code
- HST
- Recalls
- None
- Predicates
- 0
FDA’s file for it is a 510(k) statement, which names no predicate.
Sources: FDA 510(k) database (decision fields), the FDA 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in HST? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin the report
What was it cleared against?
FDA’s file for it is a 510(k) statement, which names no predicate.
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
How does its category compare?
All HST devicesHST Apparatus, Traction, Non-Powered: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · HST
1in 2016
2026 to Oct 25, outlined.
Median 510(k) review, days · HST
Too few HST 510(k)s in any year since 2007 to give a median.
Recalls per year · HST
1in 2016
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · HST
20in 2025
MAUDE reports naming product code HST, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 0 | 1 |
| 2008 | 0 | — | 0 | 4 |
| 2009 | 0 | — | 2 | 28 |
| 2010 | 0 | — | 0 | 2 |
| 2011 | 1 | — | 0 | 1 |
| 2012 | 0 | — | 0 | 5 |
| 2013 | 0 | — | 1 | 49 |
| 2014 | 0 | — | 2 | 38 |
| 2015 | 0 | — | 0 | 37 |
| 2016 | 1 | — | 1 | 28 |
| 2017 | 0 | — | 0 | 20 |
| 2018 | 0 | — | 0 | 25 |
| 2019 | 0 | — | 0 | 32 |
| 2020 | 0 | — | 0 | 37 |
| 2021 | 0 | — | 0 | 40 |
| 2022 | 0 | — | 0 | 26 |
| 2023 | 0 | — | 0 | 18 |
| 2024 | 0 | — | 0 | 47 |
| 2025 | 0 | — | 0 | 20 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The BACK-ON-TRAC is intended for the treatment of acute and chronic low back pain of disc origin or due to malalignments of the apophyseal joints.
Indications for use read by OCR from a scanned FDA 510(k) statement, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K984190 · printed Nov 5, 2026
Cite this page
510(k) Report. “K984190: Back-on-Trac, Model 101BOT.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K984190
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Page last updated Nov 3, 2026