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FDA 510(k)

ARTHREX FINGERSHIELD FINGER GUARD, MODEL AR-7199-XX

K-Number: K052387 · 2005-11-29

ApplicantArthrex, Inc.
Decision Date2005-11-29
Product CodeLZB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ARTHREX FINGERSHIELD FINGER GUARD, MODEL AR-7199-XX is the device name listed in this FDA 510(k) record. The listed applicant is Arthrex, Inc.. It received FDA 510(k) clearance on 2005-11-29 under 510(k) number K052387. The device is classified under product code LZB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHREX FINGERSHIELD FINGER GUARD, MODEL AR-7199-XX?

ARTHREX FINGERSHIELD FINGER GUARD, MODEL AR-7199-XX is a medical device that received FDA 510(k) clearance on 2005-11-29. The listed applicant is Arthrex, Inc.. The 510(k) number is K052387.

When did ARTHREX FINGERSHIELD FINGER GUARD, MODEL AR-7199-XX receive FDA 510(k) clearance?

ARTHREX FINGERSHIELD FINGER GUARD, MODEL AR-7199-XX received FDA 510(k) clearance on 2005-11-29, under 510(k) number K052387.

Who is the listed applicant for ARTHREX FINGERSHIELD FINGER GUARD, MODEL AR-7199-XX?

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 ARTHREX FINGERSHIELD FINGER GUARD, MODEL AR-7199-XX?

The FDA product code for ARTHREX FINGERSHIELD FINGER GUARD, MODEL AR-7199-XX is LZB.

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Related Devices (Code: LZB)

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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