FDA 510(k)

MODIFICATION TO ARTHROCARE ARTHROWANDS

K-Number: K070958 · 2007-04-23

Decision Date2007-04-23

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO ARTHROCARE ARTHROWANDS is the device name listed in this FDA 510(k) record. The listed applicant is Arthrocare Corp.. It received FDA 510(k) clearance on 2007-04-23 under 510(k) number K070958. 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 MODIFICATION TO ARTHROCARE ARTHROWANDS?

MODIFICATION TO ARTHROCARE ARTHROWANDS is a medical device that received FDA 510(k) clearance on 2007-04-23. The listed applicant is Arthrocare Corp.. The 510(k) number is K070958.

When did MODIFICATION TO ARTHROCARE ARTHROWANDS receive FDA 510(k) clearance?

MODIFICATION TO ARTHROCARE ARTHROWANDS received FDA 510(k) clearance on 2007-04-23, under 510(k) number K070958.

Who is the listed applicant for MODIFICATION TO ARTHROCARE ARTHROWANDS?

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

What is the FDA product code for MODIFICATION TO ARTHROCARE ARTHROWANDS?

The FDA product code for MODIFICATION TO ARTHROCARE ARTHROWANDS is GEI.

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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.