TRITON/TRU-TRAC/TX/TRITON DTS TRACTION— 510(k) K053223

Name: FDA 510(k) clearance K053223
Creator: U.S. Food and Drug Administration
Published: 2006-02-24

Substantially Equivalent

Chattanooga Group

FDA 510(k) clearance K053223 for TRITON/TRU-TRAC/TX/TRITON DTS TRACTION, Substantially Equivalent on 2006-02-24. Applicant: Chattanooga Group. Device class: 2.

Clearance details

Applicant: Chattanooga Group
Product code: Code ITH
Device class: Class 2
Regulation: 21 CFR 890.5900
Advisory panel: Physical Medicine
Date received: 2005-11-17
Decision date: 2006-02-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hixson, TN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code ITH

view all

K243775 — True Non-Surgical Spinal Decompression System (DRX9000-SL)2025-07-18
K243366 — DRX9000C-SL Cervical Spinal Decompression System2025-06-18
K214037 — Ergo-Flex Technologies Back on Trac (BOTGEN1) and Cervi-Trac2024-02-22
K222912 — c1Trac2023-05-16
K151640 — ELTRAC 4712015-10-16

More clearances from Chattanooga Group

view all

K090632 — COMPEX REHAB2009-06-01
K083433 — INTELECT SWD 100, MODEL 1600; SENIOR SOLUTIONS SHORTWAVE DIATHERMY, MODEL 16012009-03-18
K083140 — COMPEX SPORT PLUS2009-02-09
K070425 — VITALSTIM EXPERIA2007-06-11
K051938 — TRITON/TRU-TRAC/TX TRACTION DEVICES2005-09-21

Data sourced from openFDA. This site is unofficial and independent of the FDA.