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FDA 510(k)

ArthrexVIP Web Portal

K-Number: K193523 · 2020-04-30

ApplicantArthrex, Inc.
Decision Date2020-04-30
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ArthrexVIP Web Portal is a medical device manufactured by Arthrex, Inc.. It received FDA 510(k) clearance on 2020-04-30 under approval number K193523. 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 ArthrexVIP Web Portal?

ArthrexVIP Web Portal is a medical device that received FDA 510(k) clearance on 2020-04-30. It is manufactured by Arthrex, Inc.. The 510(k) number is K193523.

When was ArthrexVIP Web Portal approved by the FDA?

ArthrexVIP Web Portal received FDA 510(k) clearance on 2020-04-30, under approval number K193523.

What company makes ArthrexVIP Web Portal?

ArthrexVIP Web Portal is manufactured by Arthrex, Inc..

What is the FDA product code for ArthrexVIP Web Portal?

The FDA product code for ArthrexVIP Web Portal is LLZ.

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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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