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FDA 510(k)

ARTHREX INSTRUMENTS ( HIP )

K-Number: K926212 · 1994-01-31

ApplicantArthrex, Inc.
Decision Date1994-01-31
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARTHREX INSTRUMENTS ( HIP ) is the device name listed in this FDA 510(k) record. The listed applicant is Arthrex, Inc.. It received FDA 510(k) clearance on 1994-01-31 under 510(k) number K926212. 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 ARTHREX INSTRUMENTS ( HIP )?

ARTHREX INSTRUMENTS ( HIP ) is a medical device that received FDA 510(k) clearance on 1994-01-31. The listed applicant is Arthrex, Inc.. The 510(k) number is K926212.

When did ARTHREX INSTRUMENTS ( HIP ) receive FDA 510(k) clearance?

ARTHREX INSTRUMENTS ( HIP ) received FDA 510(k) clearance on 1994-01-31, under 510(k) number K926212.

Who is the listed applicant for ARTHREX INSTRUMENTS ( HIP )?

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 INSTRUMENTS ( HIP )?

The FDA product code for ARTHREX INSTRUMENTS ( HIP ) is HRX.

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Other records listing Arthrex, 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.

K262975Arthrex Beaming SystemK262618Arthrex Spine Compression FT ScrewK262451Arthrex DynaNite StaplesK262357Arthrex Bioabsorbable PushLock Suture AnchorsK260624Arthrex Radial Head Replacement SystemK260018Arthrex FiberButton

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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.

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

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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