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FDA 510(k)

KSEA LARGE JOINT ARTHROSCOPY SET

K-Number: K963524 · 1996-11-14

ApplicantKarl Storz Endoscopy
Decision Date1996-11-14
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KSEA LARGE JOINT ARTHROSCOPY SET is the device name listed in this FDA 510(k) record. The listed applicant is Karl Storz Endoscopy. It received FDA 510(k) clearance on 1996-11-14 under 510(k) number K963524. 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 KSEA LARGE JOINT ARTHROSCOPY SET?

KSEA LARGE JOINT ARTHROSCOPY SET is a medical device that received FDA 510(k) clearance on 1996-11-14. The listed applicant is Karl Storz Endoscopy. The 510(k) number is K963524.

When did KSEA LARGE JOINT ARTHROSCOPY SET receive FDA 510(k) clearance?

KSEA LARGE JOINT ARTHROSCOPY SET received FDA 510(k) clearance on 1996-11-14, under 510(k) number K963524.

Who is the listed applicant for KSEA LARGE JOINT ARTHROSCOPY SET?

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

What is the FDA product code for KSEA LARGE JOINT ARTHROSCOPY SET?

The FDA product code for KSEA LARGE JOINT ARTHROSCOPY SET is HRX.

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Other records listing Karl Storz Endoscopy 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.

K043375FISCH TITANIUM MIDDLE EAR PROSTHESESK030848PERFORATED BIOABSORBABLE INTERFERENCE SCREW MEGAFIXK030009KSEA POWERSHAVER SYSTEM S2K023924AUTOCON II 200 ELECTROSURGICAL GENERATORK023187KSEA SPINOSCOPEK011700MODULITH SLK LITHOTRIPTER

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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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