FDA 510(k)

SMITH + NEPHEW RF ARTHROSCOPIC WAND SYSTEM

K-Number: K001226 · 2000-06-26

Decision Date2000-06-26

Product CodeHRX

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

SMITH + NEPHEW RF ARTHROSCOPIC WAND SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2000-06-26 under 510(k) number K001226. 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 SMITH + NEPHEW RF ARTHROSCOPIC WAND SYSTEM?

SMITH + NEPHEW RF ARTHROSCOPIC WAND SYSTEM is a medical device that received FDA 510(k) clearance on 2000-06-26. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K001226.

When did SMITH + NEPHEW RF ARTHROSCOPIC WAND SYSTEM receive FDA 510(k) clearance?

SMITH + NEPHEW RF ARTHROSCOPIC WAND SYSTEM received FDA 510(k) clearance on 2000-06-26, under 510(k) number K001226.

Who is the listed applicant for SMITH + NEPHEW RF ARTHROSCOPIC WAND SYSTEM?

The FDA 510(k) record lists Smith & Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SMITH + NEPHEW RF ARTHROSCOPIC WAND SYSTEM?

The FDA product code for SMITH + NEPHEW RF ARTHROSCOPIC WAND SYSTEM is HRX.

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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.