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FDA 510(k)

MEDIAL ROTATION KNEE SYSTEM

K-Number: K020214 · 2002-02-26

ApplicantEngineering Consulting Services, Inc.
Decision Date2002-02-26
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MEDIAL ROTATION KNEE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Engineering Consulting Services, Inc.. It received FDA 510(k) clearance on 2002-02-26 under 510(k) number K020214. 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 MEDIAL ROTATION KNEE SYSTEM?

MEDIAL ROTATION KNEE SYSTEM is a medical device that received FDA 510(k) clearance on 2002-02-26. The listed applicant is Engineering Consulting Services, Inc.. The 510(k) number is K020214.

When did MEDIAL ROTATION KNEE SYSTEM receive FDA 510(k) clearance?

MEDIAL ROTATION KNEE SYSTEM received FDA 510(k) clearance on 2002-02-26, under 510(k) number K020214.

Who is the listed applicant for MEDIAL ROTATION KNEE SYSTEM?

The FDA 510(k) record lists Engineering Consulting Services, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDIAL ROTATION KNEE SYSTEM?

The FDA product code for MEDIAL ROTATION KNEE SYSTEM is 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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