TRX VERTICAL POSITIONER
K-Number: K023426 · 2002-11-21
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Device Summary
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.
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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