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FDA 510(k)

XVWeb 3D

K-Number: K182815 · 2018-11-30

ApplicantApteryx, Inc.
Decision Date2018-11-30
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

XVWeb 3D is a medical device manufactured by Apteryx, Inc.. It received FDA 510(k) clearance on 2018-11-30 under approval number K182815. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XVWeb 3D?

XVWeb 3D is a medical device that received FDA 510(k) clearance on 2018-11-30. It is manufactured by Apteryx, Inc.. The 510(k) number is K182815.

When was XVWeb 3D approved by the FDA?

XVWeb 3D received FDA 510(k) clearance on 2018-11-30, under approval number K182815.

What company makes XVWeb 3D?

XVWeb 3D is manufactured by Apteryx, Inc..

What is the FDA product code for XVWeb 3D?

The FDA product code for XVWeb 3D is LLZ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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