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FDA 510(k)

ARTHROPLAST & ARTHRO-CUTTER

K-Number: K954217 · 1995-10-23

ApplicantFuture Medical Systems, Inc.
Decision Date1995-10-23
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARTHROPLAST & ARTHRO-CUTTER is the device name listed in this FDA 510(k) record. The listed applicant is Future Medical Systems, Inc.. It received FDA 510(k) clearance on 1995-10-23 under 510(k) number K954217. 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 ARTHROPLAST & ARTHRO-CUTTER?

ARTHROPLAST & ARTHRO-CUTTER is a medical device that received FDA 510(k) clearance on 1995-10-23. The listed applicant is Future Medical Systems, Inc.. The 510(k) number is K954217.

When did ARTHROPLAST & ARTHRO-CUTTER receive FDA 510(k) clearance?

ARTHROPLAST & ARTHRO-CUTTER received FDA 510(k) clearance on 1995-10-23, under 510(k) number K954217.

Who is the listed applicant for ARTHROPLAST & ARTHRO-CUTTER?

The FDA 510(k) record lists Future Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARTHROPLAST & ARTHRO-CUTTER?

The FDA product code for ARTHROPLAST & ARTHRO-CUTTER is HRX.

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Other records listing Future Medical Systems, Inc. as applicant

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K023963ADHOC CLAWK021030TITANIUM CANNULATED INTERFERENCE SCREWK013685PLLA CANNULATED INTERFERENCE SCREWK002040FMS SOLOK980808ENDO FMS UROLOGYK955500FMS ARTHOPROBE

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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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