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FDA 510(k)

REPROCESSED ARTHROSCOPIC SHAPERS

K-Number: K012667 · 2002-06-03

ApplicantSurgical Instruments Service and Savings, Inc.
Decision Date2002-06-03
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

REPROCESSED ARTHROSCOPIC SHAPERS is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Instruments Service and Savings, Inc.. It received FDA 510(k) clearance on 2002-06-03 under 510(k) number K012667. 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 REPROCESSED ARTHROSCOPIC SHAPERS?

REPROCESSED ARTHROSCOPIC SHAPERS is a medical device that received FDA 510(k) clearance on 2002-06-03. The listed applicant is Surgical Instruments Service and Savings, Inc.. The 510(k) number is K012667.

When did REPROCESSED ARTHROSCOPIC SHAPERS receive FDA 510(k) clearance?

REPROCESSED ARTHROSCOPIC SHAPERS received FDA 510(k) clearance on 2002-06-03, under 510(k) number K012667.

Who is the listed applicant for REPROCESSED ARTHROSCOPIC SHAPERS?

The FDA 510(k) record lists Surgical Instruments Service and Savings, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REPROCESSED ARTHROSCOPIC SHAPERS?

The FDA product code for REPROCESSED ARTHROSCOPIC SHAPERS is HRX.

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Other records listing Surgical Instruments Service and Savings, 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.

K031869SISS INC. (D.B.A. MEDISISS) REPROCESSED ELECTROSURGICAL INSTRUMENTS AND ACCESSORIESK030179MEDISISS PHACOEMULSIFICATION TIPS/NEEDLESK024011SISS REPROCESSED HOT BIOPSY FORCEPS, LAPAROSCOPIC, ENDOSCOPIC AND ELECTROSURGICAL SURGICAL INSTRUMENTS AND ACCESSORIESK012644REPROCESSED TROCARS AND CANNULASK012669REPROCESSED ELECTROSURGICAL ELECTRODESK012658REPROCESSED COMPRESSION LIMB SLEEVES

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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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