FDA 510(k)

36MM V40 FEMORAL HEAD COMPONENTS (LFIT AND NON-LFIT)

K-Number: K022077 · 2002-07-25

Decision Date2002-07-25

Product CodeJDI

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

36MM V40 FEMORAL HEAD COMPONENTS (LFIT AND NON-LFIT) 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 2002-07-25 under 510(k) number K022077. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 36MM V40 FEMORAL HEAD COMPONENTS (LFIT AND NON-LFIT)?

36MM V40 FEMORAL HEAD COMPONENTS (LFIT AND NON-LFIT) is a medical device that received FDA 510(k) clearance on 2002-07-25. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K022077.

When did 36MM V40 FEMORAL HEAD COMPONENTS (LFIT AND NON-LFIT) receive FDA 510(k) clearance?

36MM V40 FEMORAL HEAD COMPONENTS (LFIT AND NON-LFIT) received FDA 510(k) clearance on 2002-07-25, under 510(k) number K022077.

Who is the listed applicant for 36MM V40 FEMORAL HEAD COMPONENTS (LFIT AND NON-LFIT)?

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 36MM V40 FEMORAL HEAD COMPONENTS (LFIT AND NON-LFIT)?

The FDA product code for 36MM V40 FEMORAL HEAD COMPONENTS (LFIT AND NON-LFIT) is JDI.

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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.