FDA 510(k)

UNIVERSAL CMF SYSTEM

K-Number: K022185 · 2002-12-17

Decision Date2002-12-17

Product CodeJEY

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

UNIVERSAL CMF SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Instruments. It received FDA 510(k) clearance on 2002-12-17 under 510(k) number K022185. The device is classified under product code JEY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIVERSAL CMF SYSTEM?

UNIVERSAL CMF SYSTEM is a medical device that received FDA 510(k) clearance on 2002-12-17. The listed applicant is Stryker Instruments. The 510(k) number is K022185.

When did UNIVERSAL CMF SYSTEM receive FDA 510(k) clearance?

UNIVERSAL CMF SYSTEM received FDA 510(k) clearance on 2002-12-17, under 510(k) number K022185.

Who is the listed applicant for UNIVERSAL CMF SYSTEM?

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

What is the FDA product code for UNIVERSAL CMF SYSTEM?

The FDA product code for UNIVERSAL CMF SYSTEM is JEY.

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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.