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FDA 510(k)

DURACON INSET PATELLA, 25MM

K-Number: K993692 · 1999-12-02

ApplicantHowmedica Osteonics Corp.
Decision Date1999-12-02
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DURACON INSET PATELLA, 25MM is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Osteonics Corp.. It received FDA 510(k) clearance on 1999-12-02 under 510(k) number K993692. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DURACON INSET PATELLA, 25MM?

DURACON INSET PATELLA, 25MM is a medical device that received FDA 510(k) clearance on 1999-12-02. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K993692.

When did DURACON INSET PATELLA, 25MM receive FDA 510(k) clearance?

DURACON INSET PATELLA, 25MM received FDA 510(k) clearance on 1999-12-02, under 510(k) number K993692.

Who is the listed applicant for DURACON INSET PATELLA, 25MM?

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

What is the FDA product code for DURACON INSET PATELLA, 25MM?

The FDA product code for DURACON INSET PATELLA, 25MM is JWH.

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Related Devices (Code: JWH)

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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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