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FDA 510(k)

HYDROXYAPATITE

K-Number: K842718 · 1984-11-07

ApplicantDepuy, Inc.
Decision Date1984-11-07
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HYDROXYAPATITE is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1984-11-07 under 510(k) number K842718. The device is classified under product code LYC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYDROXYAPATITE?

HYDROXYAPATITE is a medical device that received FDA 510(k) clearance on 1984-11-07. The listed applicant is Depuy, Inc.. The 510(k) number is K842718.

When did HYDROXYAPATITE receive FDA 510(k) clearance?

HYDROXYAPATITE received FDA 510(k) clearance on 1984-11-07, under 510(k) number K842718.

Who is the listed applicant for HYDROXYAPATITE?

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 HYDROXYAPATITE?

The FDA product code for HYDROXYAPATITE is LYC.

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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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