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FDA 510(k)

INTERSEGMENTAL TRACTION TABLE

K-Number: K915784 · 1992-01-14

Decision Date1992-01-14
Product CodeJFB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

INTERSEGMENTAL TRACTION TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Tjn Manufacturing,Inc.. It received FDA 510(k) clearance on 1992-01-14 under 510(k) number K915784. The device is classified under product code JFB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERSEGMENTAL TRACTION TABLE?

INTERSEGMENTAL TRACTION TABLE is a medical device that received FDA 510(k) clearance on 1992-01-14. The listed applicant is Tjn Manufacturing,Inc.. The 510(k) number is K915784.

When did INTERSEGMENTAL TRACTION TABLE receive FDA 510(k) clearance?

INTERSEGMENTAL TRACTION TABLE received FDA 510(k) clearance on 1992-01-14, under 510(k) number K915784.

Who is the listed applicant for INTERSEGMENTAL TRACTION TABLE?

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

What is the FDA product code for INTERSEGMENTAL TRACTION TABLE?

The FDA product code for INTERSEGMENTAL TRACTION TABLE is JFB.

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 Tjn Manufacturing,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.

Related Devices (Code: JFB)

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

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

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