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FDA 510(k)

VV FLUORO 3D

K-Number: K070106 · 2007-04-23

ApplicantBrainlab AG
Decision Date2007-04-23
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VV FLUORO 3D is the device name listed in this FDA 510(k) record. The listed applicant is Brainlab AG. It received FDA 510(k) clearance on 2007-04-23 under 510(k) number K070106. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VV FLUORO 3D?

VV FLUORO 3D is a medical device that received FDA 510(k) clearance on 2007-04-23. The listed applicant is Brainlab AG. The 510(k) number is K070106.

When did VV FLUORO 3D receive FDA 510(k) clearance?

VV FLUORO 3D received FDA 510(k) clearance on 2007-04-23, under 510(k) number K070106.

Who is the listed applicant for VV FLUORO 3D?

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

What is the FDA product code for VV FLUORO 3D?

The FDA product code for VV FLUORO 3D is HAW.

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Related Devices (Code: HAW)

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.

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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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