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FDA 510(k)

STRYKER HIP ARTHOROSCOPY SET

K-Number: K982375 · 1998-10-02

ApplicantStryker Endoscopy
Decision Date1998-10-02
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

STRYKER HIP ARTHOROSCOPY SET is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Endoscopy. It received FDA 510(k) clearance on 1998-10-02 under 510(k) number K982375. 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 STRYKER HIP ARTHOROSCOPY SET?

STRYKER HIP ARTHOROSCOPY SET is a medical device that received FDA 510(k) clearance on 1998-10-02. The listed applicant is Stryker Endoscopy. The 510(k) number is K982375.

When did STRYKER HIP ARTHOROSCOPY SET receive FDA 510(k) clearance?

STRYKER HIP ARTHOROSCOPY SET received FDA 510(k) clearance on 1998-10-02, under 510(k) number K982375.

Who is the listed applicant for STRYKER HIP ARTHOROSCOPY SET?

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

What is the FDA product code for STRYKER HIP ARTHOROSCOPY SET?

The FDA product code for STRYKER HIP ARTHOROSCOPY SET is HRX.

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Related Devices (Code: HRX)

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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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