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FDA 510(k)

BENCHMARK SERIES ARTHROSCCOPIC INSTRUMENTS

K-Number: K946151 · 1995-05-09

ApplicantDepuy, Inc.
Decision Date1995-05-09
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BENCHMARK SERIES ARTHROSCCOPIC INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1995-05-09 under 510(k) number K946151. 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 BENCHMARK SERIES ARTHROSCCOPIC INSTRUMENTS?

BENCHMARK SERIES ARTHROSCCOPIC INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1995-05-09. The listed applicant is Depuy, Inc.. The 510(k) number is K946151.

When did BENCHMARK SERIES ARTHROSCCOPIC INSTRUMENTS receive FDA 510(k) clearance?

BENCHMARK SERIES ARTHROSCCOPIC INSTRUMENTS received FDA 510(k) clearance on 1995-05-09, under 510(k) number K946151.

Who is the listed applicant for BENCHMARK SERIES ARTHROSCCOPIC INSTRUMENTS?

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

What is the FDA product code for BENCHMARK SERIES ARTHROSCCOPIC INSTRUMENTS?

The FDA product code for BENCHMARK SERIES ARTHROSCCOPIC INSTRUMENTS is HRX.

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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.

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