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FDA 510(k)

HOFFMANN II COMPACT PERIARTICULAR CLAMP

K-Number: K973321 · 1997-11-20

ApplicantHowmedica, Inc.
Decision Date1997-11-20
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HOFFMANN II COMPACT PERIARTICULAR CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica, Inc.. It received FDA 510(k) clearance on 1997-11-20 under 510(k) number K973321. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOFFMANN II COMPACT PERIARTICULAR CLAMP?

HOFFMANN II COMPACT PERIARTICULAR CLAMP is a medical device that received FDA 510(k) clearance on 1997-11-20. The listed applicant is Howmedica, Inc.. The 510(k) number is K973321.

When did HOFFMANN II COMPACT PERIARTICULAR CLAMP receive FDA 510(k) clearance?

HOFFMANN II COMPACT PERIARTICULAR CLAMP received FDA 510(k) clearance on 1997-11-20, under 510(k) number K973321.

Who is the listed applicant for HOFFMANN II COMPACT PERIARTICULAR CLAMP?

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

What is the FDA product code for HOFFMANN II COMPACT PERIARTICULAR CLAMP?

The FDA product code for HOFFMANN II COMPACT PERIARTICULAR CLAMP is KTT.

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Other records listing Howmedica, Inc. as applicant

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Related Devices (Code: KTT)

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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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