Cervitrac Traction Frame & Cord

FDA 510(k) K821522 · George W. Cottrell

Substantially Equivalent

510(k) numberK821522

Submission

Device name
Cervitrac Traction Frame & Cord
Applicant
George W. Cottrell
Walker, MI, US
Received
May 17, 1982
Decision date
June 21, 1982
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 Cervitrac Traction Frame & Cord cleared by the FDA?

Cervitrac Traction Frame & Cord (K821522) received a 510(k) decision of Substantially Equivalent on June 21, 1982, 35 days after the submission was received.

What is the product code of K821522?

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