X-TRA BASE
K-Number: K123773 · 2012-12-21
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Device Summary
Frequently Asked Questions
What is the X-TRA BASE?
X-TRA BASE is a medical device that received FDA 510(k) clearance on 2012-12-21. The listed applicant is Voco GmbH. The 510(k) number is K123773.
When did X-TRA BASE receive FDA 510(k) clearance?
X-TRA BASE received FDA 510(k) clearance on 2012-12-21, under 510(k) number K123773.
Who is the listed applicant for X-TRA BASE?
The FDA 510(k) record lists Voco GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for X-TRA BASE?
The FDA product code for X-TRA BASE is EBF.
Other records listing Voco GmbH 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: EBF)
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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