Isotechnologies Back Tracker and Back Works Softwa

FDA 510(k) K933063 · Isotechnologies, Inc.

Substantially Equivalent

510(k) numberK933063

Submission

Device name
Isotechnologies Back Tracker and Back Works Softwa
Applicant
Isotechnologies, Inc.
Hillsborough, NC, US
Received
June 22, 1993
Decision date
January 27, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
KQX – Goniometer, Ac-Powered
Device class
Class I (low risk)
Regulation
21 CFR 888.1500
Specialty
Orthopedic

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K9623773D-SPINEKQX · Traditional Skill Technologies, Inc.09/03/1996SE
K961212Spinal TouchKQX · Traditional Fasstech06/12/1996SE
K954647InclinometerKQX · Traditional J-Tech, Inc.10/30/1995SE
K943929Dataglove and Movement Analysis System (Mas)KQX · Traditional Greenleaf Medical Systems, Inc.05/15/1995SE
K945630Large Muscle Strength GaugeKQX · Traditional J-Tech, Inc.05/10/1995SE
K943898Saunders Electronic InclinometerKQX · Traditional The Saunders Group11/28/1994SE
K940812Insight Electronic Alignment IndicatorKQX · Traditional Andronic Devices, Ltd.11/21/1994SE
K925225The Bte Vector; Analysis System for the Low BackKQX · Traditional Baltimore Therapeutic Equipment Co.06/27/1994SE

More from Baltimore Therapeutic Equipment Co.

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K912175Isotechnologies Liftstation & Liftworks SoftwareINK · Traditional 06/07/1991SE
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K844060Isostation Ankle/Subtalar Machine A-100IKK · Traditional 11/23/1984SE
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Questions and answers

When was Isotechnologies Back Tracker and Back Works Softwa cleared by the FDA?

Isotechnologies Back Tracker and Back Works Softwa (K933063) received a 510(k) decision of Substantially Equivalent on January 27, 1994, 219 days after the submission was received.

What is the product code of K933063?

The FDA product code is KQX – Goniometer, Ac-Powered, a Class I (low risk) device regulated under 21 CFR 888.1500.