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FDA 510(k)

ATHROCARE TOPAZ ARTHROWANDS

K-Number: K053567 · 2006-03-06

ApplicantArthrocare Corp.
Decision Date2006-03-06
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ATHROCARE TOPAZ 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 2006-03-06 under 510(k) number K053567. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATHROCARE TOPAZ ARTHROWANDS?

ATHROCARE TOPAZ ARTHROWANDS is a medical device that received FDA 510(k) clearance on 2006-03-06. The listed applicant is Arthrocare Corp.. The 510(k) number is K053567.

When did ATHROCARE TOPAZ ARTHROWANDS receive FDA 510(k) clearance?

ATHROCARE TOPAZ ARTHROWANDS received FDA 510(k) clearance on 2006-03-06, under 510(k) number K053567.

Who is the listed applicant for ATHROCARE TOPAZ 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 ATHROCARE TOPAZ ARTHROWANDS?

The FDA product code for ATHROCARE TOPAZ ARTHROWANDS is HRX.

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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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