Medi-Trak Portable Traction Device

FDA 510(k) K791396 · Medicorp, Inc.

Substantially Equivalent

510(k) numberK791396

Submission

Device name
Medi-Trak Portable Traction Device
Applicant
Medicorp, Inc.
Mchenry, IL, US
Received
July 10, 1979
Decision date
August 16, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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
K984190Back-On-Trac, Model 101BOTHST · Traditional Back-On-Track, Inc.03/15/1999SE
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

More from Comfortex, Inc.

510(k)DeviceDecision
K860026Ultramax III, Dialyzer Reprocessing DeviceLIF · Traditional 03/14/1986SE
K844850Medicorp Dehydracon a Dehydrated Dialysate ConcentFKQ · Traditional 04/02/1985SE
K832705UltramaxLIF · Traditional 06/25/1984SE
K791164Negatove Pressure ConvertorFLC · Traditional 10/04/1979SE

Questions and answers

When was Medi-Trak Portable Traction Device cleared by the FDA?

Medi-Trak Portable Traction Device (K791396) received a 510(k) decision of Substantially Equivalent on August 16, 1979, 37 days after the submission was received.

What is the product code of K791396?

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