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FDA 510(k)

SEARCH EVOLUTION TOTAL KNEE SYSTEM

K-Number: K021313 · 2002-07-22

ApplicantAesculap, Inc.
Decision Date2002-07-22
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SEARCH EVOLUTION TOTAL KNEE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2002-07-22 under 510(k) number K021313. 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 SEARCH EVOLUTION TOTAL KNEE SYSTEM?

SEARCH EVOLUTION TOTAL KNEE SYSTEM is a medical device that received FDA 510(k) clearance on 2002-07-22. The listed applicant is Aesculap, Inc.. The 510(k) number is K021313.

When did SEARCH EVOLUTION TOTAL KNEE SYSTEM receive FDA 510(k) clearance?

SEARCH EVOLUTION TOTAL KNEE SYSTEM received FDA 510(k) clearance on 2002-07-22, under 510(k) number K021313.

Who is the listed applicant for SEARCH EVOLUTION TOTAL KNEE SYSTEM?

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

What is the FDA product code for SEARCH EVOLUTION TOTAL KNEE SYSTEM?

The FDA product code for SEARCH EVOLUTION TOTAL KNEE SYSTEM 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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