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FDA 510(k)

CTBOX CERVICAL/LUMBAR TRACTION

K-Number: K063353 · 2007-03-14

ApplicantCircular Traction Supply, Inc.
Decision Date2007-03-14
Product CodeITH
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CTBOX CERVICAL/LUMBAR TRACTION is the device name listed in this FDA 510(k) record. The listed applicant is Circular Traction Supply, Inc.. It received FDA 510(k) clearance on 2007-03-14 under 510(k) number K063353. 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 CTBOX CERVICAL/LUMBAR TRACTION?

CTBOX CERVICAL/LUMBAR TRACTION is a medical device that received FDA 510(k) clearance on 2007-03-14. The listed applicant is Circular Traction Supply, Inc.. The 510(k) number is K063353.

When did CTBOX CERVICAL/LUMBAR TRACTION receive FDA 510(k) clearance?

CTBOX CERVICAL/LUMBAR TRACTION received FDA 510(k) clearance on 2007-03-14, under 510(k) number K063353.

Who is the listed applicant for CTBOX CERVICAL/LUMBAR TRACTION?

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

What is the FDA product code for CTBOX CERVICAL/LUMBAR TRACTION?

The FDA product code for CTBOX CERVICAL/LUMBAR 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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