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FDA 510(k)

TRITON/TRU-TRAC/TX/TRITON DTS TRACTION

K-Number: K053223 · 2006-02-24

ApplicantChattanooga Group
Decision Date2006-02-24
Product CodeITH
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TRITON/TRU-TRAC/TX/TRITON DTS TRACTION is the device name listed in this FDA 510(k) record. The listed applicant is Chattanooga Group. It received FDA 510(k) clearance on 2006-02-24 under 510(k) number K053223. The device is classified under product code ITH. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRITON/TRU-TRAC/TX/TRITON DTS TRACTION?

TRITON/TRU-TRAC/TX/TRITON DTS TRACTION is a medical device that received FDA 510(k) clearance on 2006-02-24. The listed applicant is Chattanooga Group. The 510(k) number is K053223.

When did TRITON/TRU-TRAC/TX/TRITON DTS TRACTION receive FDA 510(k) clearance?

TRITON/TRU-TRAC/TX/TRITON DTS TRACTION received FDA 510(k) clearance on 2006-02-24, under 510(k) number K053223.

Who is the listed applicant for TRITON/TRU-TRAC/TX/TRITON DTS TRACTION?

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

What is the FDA product code for TRITON/TRU-TRAC/TX/TRITON DTS TRACTION?

The FDA product code for TRITON/TRU-TRAC/TX/TRITON DTS TRACTION is ITH.

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Related Devices (Code: ITH)

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.

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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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