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FDA 510(k)

CANNULA MODEL AR-6001

K-Number: K880295 · 1988-06-29

ApplicantArthrex Arthroscopy Instruments, Inc.
Decision Date1988-06-29
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CANNULA MODEL AR-6001 is the device name listed in this FDA 510(k) record. The listed applicant is Arthrex Arthroscopy Instruments, Inc.. It received FDA 510(k) clearance on 1988-06-29 under 510(k) number K880295. 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 CANNULA MODEL AR-6001?

CANNULA MODEL AR-6001 is a medical device that received FDA 510(k) clearance on 1988-06-29. The listed applicant is Arthrex Arthroscopy Instruments, Inc.. The 510(k) number is K880295.

When did CANNULA MODEL AR-6001 receive FDA 510(k) clearance?

CANNULA MODEL AR-6001 received FDA 510(k) clearance on 1988-06-29, under 510(k) number K880295.

Who is the listed applicant for CANNULA MODEL AR-6001?

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

What is the FDA product code for CANNULA MODEL AR-6001?

The FDA product code for CANNULA MODEL AR-6001 is HRX.

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Other records listing Arthrex Arthroscopy Instruments, Inc. as applicant

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.

K881792CANNULA MODEL AR-6551

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.

K260203Fule Vertebroplasty Balloon CatheterBeijing Fule Science & Technology Development Co., Ltd.K254103HOPKINS Telescopes for ArthroscopyKarl Storz SE & CO. KGK252790Digital ClarusScope System and Digital NeuroPEN SystemClarus Medical, LLCK253523Freedom DS™ Decompression SystemSpinal SimplicityK252546VantageTM Lumbar Decompression KitAllevion Medical, LLCK253217MiiS Horus Arthroscope (EJA 100); MiiS Horus Endoscope Display System -Tablet (EDS 500); MiiS Horus Endoscope Display System -Video Box (EVS 700)Medimaging Integrated Solution, Inc (Miis)

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.

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