Back-On-Trac, Model 101BOT

FDA 510(k) K984190 · Back-On-Track, Inc.

Substantially Equivalent

510(k) numberK984190

Submission

Device name
Back-On-Trac, Model 101BOT
Applicant
Back-On-Track, Inc.
St. Charles, MO, US
Received
November 23, 1998
Decision date
March 15, 1999
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
HST – Apparatus, Traction, Non-Powered
Device class
Class I (low risk)
Regulation
21 CFR 888.5850
Specialty
Orthopedic

Other 510(k)s with product code HST

510(k)DeviceApplicantDecision
K162702Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation…HST · Traditional Stl International, Inc.12/30/2016SE
K110858Lo-Bak TraxHST · Traditional Roland F Berthiaume, DC08/02/2011SE
K872121K and D Home TractHST · Traditional Joseph A. Kott, M.D.08/12/1987SE
K870212Arthroscopic Shoulder HolderHST · Traditional Dyonics, Inc.02/20/1987SE
K870125Extremity ElevatorHST · Traditional Orthopedic Systems, Inc.02/04/1987SE
K870102Tupper TrolleyHST · Traditional Orthopedic Systems, Inc.02/03/1987SE
K864765Model 668, Traction Splint, AdultHST · Traditional Ferno-Washington, Inc.12/17/1986SE
K862874The Towered 90/90 UnitHST · Traditional Lossing Orthopedic, Inc.08/07/1986SE
K860037Suspender Orthopedic Suspension DeviceHST · Traditional Comfortex, Inc.01/21/1986SE
K855179Transfer-Trax (TM) Splint TractionHST · Traditional Comfortex, Inc.01/21/1986SE

Questions and answers

When was Back-On-Trac, Model 101BOT cleared by the FDA?

Back-On-Trac, Model 101BOT (K984190) received a 510(k) decision of Substantially Equivalent on March 15, 1999, 112 days after the submission was received.

What is the product code of K984190?

The FDA product code is HST – Apparatus, Traction, Non-Powered, a Class I (low risk) device regulated under 21 CFR 888.5850.