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FDA 510(k)

MODIFICATION TO VALEO VBR

K-Number: K073505 · 2008-01-09

ApplicantAmedica Corp.
Decision Date2008-01-09
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO VALEO VBR is the device name listed in this FDA 510(k) record. The listed applicant is Amedica Corp.. It received FDA 510(k) clearance on 2008-01-09 under 510(k) number K073505. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO VALEO VBR?

MODIFICATION TO VALEO VBR is a medical device that received FDA 510(k) clearance on 2008-01-09. The listed applicant is Amedica Corp.. The 510(k) number is K073505.

When did MODIFICATION TO VALEO VBR receive FDA 510(k) clearance?

MODIFICATION TO VALEO VBR received FDA 510(k) clearance on 2008-01-09, under 510(k) number K073505.

Who is the listed applicant for MODIFICATION TO 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 MODIFICATION TO VALEO VBR?

The FDA product code for MODIFICATION TO VALEO VBR is MQP.

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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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