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FDA 510(k)

ARTHROCARE TURBINATOR WAND

K-Number: K122652 · 2013-07-02

ApplicantArthroCare Corporation
Decision Date2013-07-02
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ARTHROCARE TURBINATOR WAND is the device name listed in this FDA 510(k) record. The listed applicant is ArthroCare Corporation. It received FDA 510(k) clearance on 2013-07-02 under 510(k) number K122652. 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 ARTHROCARE TURBINATOR WAND?

ARTHROCARE TURBINATOR WAND is a medical device that received FDA 510(k) clearance on 2013-07-02. The listed applicant is ArthroCare Corporation. The 510(k) number is K122652.

When did ARTHROCARE TURBINATOR WAND receive FDA 510(k) clearance?

ARTHROCARE TURBINATOR WAND received FDA 510(k) clearance on 2013-07-02, under 510(k) number K122652.

Who is the listed applicant for ARTHROCARE TURBINATOR WAND?

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

What is the FDA product code for ARTHROCARE TURBINATOR WAND?

The FDA product code for ARTHROCARE TURBINATOR WAND is GEI.

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Related Devices (Code: 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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