FDA 510(k)

ARTHROSCOPE OPERATIVE KNIFE SET

K-Number: K771851 · 1977-10-27

ApplicantRichard Wolf Medical Instruments Corp.

Decision Date1977-10-27

Product CodeHTS

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

ARTHROSCOPE OPERATIVE KNIFE SET is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 1977-10-27 under 510(k) number K771851. The device is classified under product code HTS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHROSCOPE OPERATIVE KNIFE SET?

ARTHROSCOPE OPERATIVE KNIFE SET is a medical device that received FDA 510(k) clearance on 1977-10-27. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K771851.

When did ARTHROSCOPE OPERATIVE KNIFE SET receive FDA 510(k) clearance?

ARTHROSCOPE OPERATIVE KNIFE SET received FDA 510(k) clearance on 1977-10-27, under 510(k) number K771851.

Who is the listed applicant for ARTHROSCOPE OPERATIVE KNIFE SET?

The FDA 510(k) record lists Richard Wolf Medical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARTHROSCOPE OPERATIVE KNIFE SET?

The FDA product code for ARTHROSCOPE OPERATIVE KNIFE SET is HTS.

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Other records listing Richard Wolf Medical Instruments Corp. as applicant

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Related Devices (Code: HTS)

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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.