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FDA 510(k)

FMS ARTHRO-CUTTER

K-Number: K951701 · 1995-05-09

ApplicantFuture Medical Systems, Inc.
Decision Date1995-05-09
Product CodeHNX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

FMS 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 1995-05-09 under 510(k) number K951701. The device is classified under product code HNX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FMS ARTHRO-CUTTER?

FMS ARTHRO-CUTTER is a medical device that received FDA 510(k) clearance on 1995-05-09. The listed applicant is Future Medical Systems, Inc.. The 510(k) number is K951701.

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

FMS ARTHRO-CUTTER received FDA 510(k) clearance on 1995-05-09, under 510(k) number K951701.

Who is the listed applicant for FMS 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 FMS ARTHRO-CUTTER?

The FDA product code for FMS ARTHRO-CUTTER is HNX.

Related Clinical Trials

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Other records listing Future Medical Systems, 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.

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

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Related Devices (Code: HNX)

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.

K951702FMS HIGH FLOW ARTHRO-SHEATHFuture Medical Systems, Inc.

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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