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FDA 510(k)

SEARCH EVOLUTION (LC) TOTAL KNEE SYSTEM (POROUS COATED)

K-Number: K032108 · 2004-01-15

ApplicantAesculap, Inc.
Decision Date2004-01-15
Product CodeMBH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SEARCH EVOLUTION (LC) TOTAL KNEE SYSTEM (POROUS COATED) is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2004-01-15 under 510(k) number K032108. The device is classified under product code MBH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEARCH EVOLUTION (LC) TOTAL KNEE SYSTEM (POROUS COATED)?

SEARCH EVOLUTION (LC) TOTAL KNEE SYSTEM (POROUS COATED) is a medical device that received FDA 510(k) clearance on 2004-01-15. The listed applicant is Aesculap, Inc.. The 510(k) number is K032108.

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

SEARCH EVOLUTION (LC) TOTAL KNEE SYSTEM (POROUS COATED) received FDA 510(k) clearance on 2004-01-15, under 510(k) number K032108.

Who is the listed applicant for SEARCH EVOLUTION (LC) TOTAL KNEE SYSTEM (POROUS COATED)?

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 (LC) TOTAL KNEE SYSTEM (POROUS COATED)?

The FDA product code for SEARCH EVOLUTION (LC) TOTAL KNEE SYSTEM (POROUS COATED) is MBH.

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Related Devices (Code: MBH)

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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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