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FDA 510(k)

TRX VERTICAL POSITIONER

K-Number: K023426 · 2002-11-21

Decision Date2002-11-21
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TRX VERTICAL POSITIONER is the device name listed in this FDA 510(k) record. The listed applicant is Motion Concepts. It received FDA 510(k) clearance on 2002-11-21 under 510(k) number K023426. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRX VERTICAL POSITIONER?

TRX VERTICAL POSITIONER is a medical device that received FDA 510(k) clearance on 2002-11-21. The listed applicant is Motion Concepts. The 510(k) number is K023426.

When did TRX VERTICAL POSITIONER receive FDA 510(k) clearance?

TRX VERTICAL POSITIONER received FDA 510(k) clearance on 2002-11-21, under 510(k) number K023426.

Who is the listed applicant for TRX VERTICAL POSITIONER?

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

What is the FDA product code for TRX VERTICAL POSITIONER?

The FDA product code for TRX VERTICAL POSITIONER is ITI.

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 Motion Concepts 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: ITI)

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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