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FDA 510(k)

BACK ON TRACK INVERSION THERAPY & EXER

K-Number: K823236 · 1983-01-21

Decision Date1983-01-21
Product CodeION
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BACK ON TRACK INVERSION THERAPY & EXER is the device name listed in this FDA 510(k) record. The listed applicant is Lossing Orthopedic, Inc.. It received FDA 510(k) clearance on 1983-01-21 under 510(k) number K823236. The device is classified under product code ION. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BACK ON TRACK INVERSION THERAPY & EXER?

BACK ON TRACK INVERSION THERAPY & EXER is a medical device that received FDA 510(k) clearance on 1983-01-21. The listed applicant is Lossing Orthopedic, Inc.. The 510(k) number is K823236.

When did BACK ON TRACK INVERSION THERAPY & EXER receive FDA 510(k) clearance?

BACK ON TRACK INVERSION THERAPY & EXER received FDA 510(k) clearance on 1983-01-21, under 510(k) number K823236.

Who is the listed applicant for BACK ON TRACK INVERSION THERAPY & EXER?

The FDA 510(k) record lists Lossing Orthopedic, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BACK ON TRACK INVERSION THERAPY & EXER?

The FDA product code for BACK ON TRACK INVERSION THERAPY & EXER is ION.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Lossing Orthopedic, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 8 devices →

Related Devices (Code: ION)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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