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FDA 510(k)

ECHELON POROUS PLUS HA HIP STEMS

K-Number: K023302 · 2002-10-25

ApplicantSmith & Nephew, Inc.
Decision Date2002-10-25
Product CodeMEH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ECHELON POROUS PLUS HA HIP STEMS is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2002-10-25 under 510(k) number K023302. The device is classified under product code MEH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ECHELON POROUS PLUS HA HIP STEMS?

ECHELON POROUS PLUS HA HIP STEMS is a medical device that received FDA 510(k) clearance on 2002-10-25. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K023302.

When did ECHELON POROUS PLUS HA HIP STEMS receive FDA 510(k) clearance?

ECHELON POROUS PLUS HA HIP STEMS received FDA 510(k) clearance on 2002-10-25, under 510(k) number K023302.

Who is the listed applicant for ECHELON POROUS PLUS HA HIP STEMS?

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

What is the FDA product code for ECHELON POROUS PLUS HA HIP STEMS?

The FDA product code for ECHELON POROUS PLUS HA HIP STEMS is MEH.

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Related Devices (Code: MEH)

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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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