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FDA 510(k)

FLOW FLEXTEND Wand (72290039)

K-Number: K254122 · 2026-03-30

ApplicantArthroCare Corporation
Decision Date2026-03-30
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FLOW FLEXTEND Wand (72290039) is a medical device manufactured by ArthroCare Corporation. It received FDA 510(k) clearance on 2026-03-30 under approval number K254122. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLOW FLEXTEND Wand (72290039)?

FLOW FLEXTEND Wand (72290039) is a medical device that received FDA 510(k) clearance on 2026-03-30. It is manufactured by ArthroCare Corporation. The 510(k) number is K254122.

When was FLOW FLEXTEND Wand (72290039) approved by the FDA?

FLOW FLEXTEND Wand (72290039) received FDA 510(k) clearance on 2026-03-30, under approval number K254122.

What company makes FLOW FLEXTEND Wand (72290039)?

FLOW FLEXTEND Wand (72290039) is manufactured by ArthroCare Corporation.

What is the FDA product code for FLOW FLEXTEND Wand (72290039)?

The FDA product code for FLOW FLEXTEND Wand (72290039) is GEI.

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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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