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FDA 510(k)

FEMORAL CEMENT REMOVAL INSTRUMENTS

K-Number: K870217 · 1987-02-06

ApplicantKenneth J. Hoek, M.D., Inc.
Decision Date1987-02-06
Product CodeHTW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FEMORAL CEMENT REMOVAL INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Kenneth J. Hoek, M.D., Inc.. It received FDA 510(k) clearance on 1987-02-06 under 510(k) number K870217. The device is classified under product code HTW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FEMORAL CEMENT REMOVAL INSTRUMENTS?

FEMORAL CEMENT REMOVAL INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1987-02-06. The listed applicant is Kenneth J. Hoek, M.D., Inc.. The 510(k) number is K870217.

When did FEMORAL CEMENT REMOVAL INSTRUMENTS receive FDA 510(k) clearance?

FEMORAL CEMENT REMOVAL INSTRUMENTS received FDA 510(k) clearance on 1987-02-06, under 510(k) number K870217.

Who is the listed applicant for FEMORAL CEMENT REMOVAL INSTRUMENTS?

The FDA 510(k) record lists Kenneth J. Hoek, M.D., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FEMORAL CEMENT REMOVAL INSTRUMENTS?

The FDA product code for FEMORAL CEMENT REMOVAL INSTRUMENTS is HTW.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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