Flexion Distration Support

FDA 510(k) K921711 · Altoona Medical Supply

Substantially Equivalent

510(k) numberK921711

Submission

Device name
Flexion Distration Support
Applicant
Altoona Medical Supply
Altoona, IA, US
Received
April 8, 1992
Decision date
July 13, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
ILZ – Accessories, Traction
Device class
Class I (low risk)
Regulation
21 CFR 890.5925
Specialty
Physical Medicine

Other 510(k)s with product code ILZ

510(k)DeviceApplicantDecision
K895382Vibra-Trac Traction TableILZ · Traditional Vibra-Trac Industries10/16/1989SE
K884340AMX-110, Amx-Ii and Amx-IiiILZ · Traditional Dyna-Med01/24/1989SE
K852398Vector Bar Suspension/Traction UnitILZ · Traditional Powlan Manufacturing Co.08/12/1985SE
K844490Traction AccessoriesILZ · Traditional Jerome Medical02/21/1985SE
K831135Saunders #7080 Cervical Traction SysILZ · Traditional Chattanooga Group, Inc.06/24/1983SE
K830245Head HalterILZ · Traditional Warm & Form, Orthopedic Materials03/09/1983SE
K823659Pelvic Traction BeltILZ · Traditional Warm & Form, Orthopedic Materials12/30/1982SE
K823166Pelvic Traction BeltILZ · Traditional Warm & Form, Orthopedic Materials11/10/1982SE
K820663Boger Auto-Traction DeviceILZ · Traditional D.C. Medical Device, Inc.05/03/1982SE
K791808Cervi-TracILZ · Traditional Dr. K.G. Rude10/01/1979SE

More from Dr. K.G. Rude

510(k)DeviceDecision
K913272EMS/400IPF · Traditional 08/22/1991SE
K893874Fujitens IIIGZQ · Traditional 12/22/1989SE

Questions and answers

When was Flexion Distration Support cleared by the FDA?

Flexion Distration Support (K921711) received a 510(k) decision of Substantially Equivalent on July 13, 1992, 96 days after the submission was received.

What is the product code of K921711?

The FDA product code is ILZ – Accessories, Traction, a Class I (low risk) device regulated under 21 CFR 890.5925.