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FDA 510(k)

Paragon T2 Wand with Integrated Cable

K-Number: K153675 · 2016-01-15

ApplicantArthroCare Corporation
Decision Date2016-01-15
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Paragon T2 Wand with Integrated Cable is a medical device manufactured by ArthroCare Corporation. It received FDA 510(k) clearance on 2016-01-15 under approval number K153675. 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 Paragon T2 Wand with Integrated Cable?

Paragon T2 Wand with Integrated Cable is a medical device that received FDA 510(k) clearance on 2016-01-15. It is manufactured by ArthroCare Corporation. The 510(k) number is K153675.

When was Paragon T2 Wand with Integrated Cable approved by the FDA?

Paragon T2 Wand with Integrated Cable received FDA 510(k) clearance on 2016-01-15, under approval number K153675.

What company makes Paragon T2 Wand with Integrated Cable?

Paragon T2 Wand with Integrated Cable is manufactured by ArthroCare Corporation.

What is the FDA product code for Paragon T2 Wand with Integrated Cable?

The FDA product code for Paragon T2 Wand with Integrated Cable is GEI.

Other Devices by ArthroCare Corporation

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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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