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FDA 510(k)

KIN-COM ASYMMETRICAL BACK SYSTEM

K-Number: K911805 · 1991-07-03

ApplicantChattanooga Group, Inc.
Decision Date1991-07-03
Product CodeIKK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

KIN-COM ASYMMETRICAL BACK SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Chattanooga Group, Inc.. It received FDA 510(k) clearance on 1991-07-03 under 510(k) number K911805. The device is classified under product code IKK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KIN-COM ASYMMETRICAL BACK SYSTEM?

KIN-COM ASYMMETRICAL BACK SYSTEM is a medical device that received FDA 510(k) clearance on 1991-07-03. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K911805.

When did KIN-COM ASYMMETRICAL BACK SYSTEM receive FDA 510(k) clearance?

KIN-COM ASYMMETRICAL BACK SYSTEM received FDA 510(k) clearance on 1991-07-03, under 510(k) number K911805.

Who is the listed applicant for KIN-COM ASYMMETRICAL BACK SYSTEM?

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

What is the FDA product code for KIN-COM ASYMMETRICAL BACK SYSTEM?

The FDA product code for KIN-COM ASYMMETRICAL BACK SYSTEM is IKK.

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Other records listing Chattanooga Group, Inc. as applicant

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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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