VALEO VBR
K-Number: K073125 · 2007-12-05
Advertisement
Device Summary
Frequently Asked Questions
What is the VALEO VBR?
VALEO VBR is a medical device that received FDA 510(k) clearance on 2007-12-05. The listed applicant is Amedica Corp.. The 510(k) number is K073125.
When did VALEO VBR receive FDA 510(k) clearance?
VALEO VBR received FDA 510(k) clearance on 2007-12-05, under 510(k) number K073125.
Who is the listed applicant for VALEO VBR?
The FDA 510(k) record lists Amedica Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VALEO VBR?
The FDA product code for VALEO VBR is MQP.
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 Amedica Corp. 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: MQP)
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.
Advertisement