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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 the device name listed in this FDA 510(k) record. The listed applicant is Apteryx, Inc.. It received FDA 510(k) clearance on 2018-11-30 under 510(k) 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. The listed applicant is Apteryx, Inc.. The 510(k) number is K182815.

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

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

Who is the listed applicant for XVWeb 3D?

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

What is the FDA product code for XVWeb 3D?

The FDA product code for XVWeb 3D is LLZ.

Related Devices (Code: LLZ)

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

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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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