Prot-A-Trac

FDA 510(k) K802072 · Robert I. Branick, M.D.

Substantially Equivalent

510(k) numberK802072

Submission

Device name
Prot-A-Trac
Applicant
Robert I. Branick, M.D.
Mchenry, IL, US
Received
August 27, 1980
Decision date
September 26, 1980
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

Questions and answers

When was Prot-A-Trac cleared by the FDA?

Prot-A-Trac (K802072) received a 510(k) decision of Substantially Equivalent on September 26, 1980, 30 days after the submission was received.

What is the product code of K802072?

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