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FDA 510(k)

ARTHROSCOPIC INSTRUMENTS

K-Number: K925456 · 1993-03-04

ApplicantArthrex, Inc.
Decision Date1993-03-04
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARTHROSCOPIC INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Arthrex, Inc.. It received FDA 510(k) clearance on 1993-03-04 under 510(k) number K925456. 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 ARTHROSCOPIC INSTRUMENTS?

ARTHROSCOPIC INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1993-03-04. The listed applicant is Arthrex, Inc.. The 510(k) number is K925456.

When did ARTHROSCOPIC INSTRUMENTS receive FDA 510(k) clearance?

ARTHROSCOPIC INSTRUMENTS received FDA 510(k) clearance on 1993-03-04, under 510(k) number K925456.

Who is the listed applicant for ARTHROSCOPIC INSTRUMENTS?

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

What is the FDA product code for ARTHROSCOPIC INSTRUMENTS?

The FDA product code for ARTHROSCOPIC INSTRUMENTS is HRX.

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Related Devices (Code: HRX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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