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FDA 510(k)

AARHUS ANCHORAGE SYSTEM

K-Number: K041527 · 2004-08-19

ApplicantMedicon EG
Decision Date2004-08-19
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

AARHUS ANCHORAGE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medicon EG. It received FDA 510(k) clearance on 2004-08-19 under 510(k) number K041527. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AARHUS ANCHORAGE SYSTEM?

AARHUS ANCHORAGE SYSTEM is a medical device that received FDA 510(k) clearance on 2004-08-19. The listed applicant is Medicon EG. The 510(k) number is K041527.

When did AARHUS ANCHORAGE SYSTEM receive FDA 510(k) clearance?

AARHUS ANCHORAGE SYSTEM received FDA 510(k) clearance on 2004-08-19, under 510(k) number K041527.

Who is the listed applicant for AARHUS ANCHORAGE SYSTEM?

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

What is the FDA product code for AARHUS ANCHORAGE SYSTEM?

The FDA product code for AARHUS ANCHORAGE SYSTEM is DZE.

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Related Devices (Code: DZE)

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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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