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FDA 510(k)

ESOP HA FEMORAL STEM

K-Number: K021108 · 2002-05-03

ApplicantFournitures Hospitalieres
Decision Date2002-05-03
Product CodeMEH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ESOP HA FEMORAL STEM is the device name listed in this FDA 510(k) record. The listed applicant is Fournitures Hospitalieres. It received FDA 510(k) clearance on 2002-05-03 under 510(k) number K021108. 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 ESOP HA FEMORAL STEM?

ESOP HA FEMORAL STEM is a medical device that received FDA 510(k) clearance on 2002-05-03. The listed applicant is Fournitures Hospitalieres. The 510(k) number is K021108.

When did ESOP HA FEMORAL STEM receive FDA 510(k) clearance?

ESOP HA FEMORAL STEM received FDA 510(k) clearance on 2002-05-03, under 510(k) number K021108.

Who is the listed applicant for ESOP HA FEMORAL STEM?

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

What is the FDA product code for ESOP HA FEMORAL STEM?

The FDA product code for ESOP HA FEMORAL STEM is MEH.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Fournitures Hospitalieres as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K021109ESOP CO-CR FEMORAL HEADSK964878ESOP S/C FEMORAL STEMK961388ATLAS III ACETABULAR CUP

Related Devices (Code: MEH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261576Icona Hip StemCorin, Ltd.K250375Allure Hip Stem and Intramedullary PlugsWaldemar Link GmbH & Co. KGK251166Mfinity Femoral SystemMedacta International S.A.K251052Trivicta® Hip StemOrtho Development Corp.K242315Resolve Modular Revision Hip StemUnited Orthopedic CorporationK243839Alteon® HA Femoral StemsExactech, Inc.

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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