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FDA 510(k)

THE LIFECORE STAGE-1 ANGLED ABUTMENT SYSTEM

K-Number: K032495 · 2003-09-17

ApplicantLifecore Biomedical, Inc.
Decision Date2003-09-17
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

THE LIFECORE STAGE-1 ANGLED ABUTMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Lifecore Biomedical, Inc.. It received FDA 510(k) clearance on 2003-09-17 under 510(k) number K032495. 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 THE LIFECORE STAGE-1 ANGLED ABUTMENT SYSTEM?

THE LIFECORE STAGE-1 ANGLED ABUTMENT SYSTEM is a medical device that received FDA 510(k) clearance on 2003-09-17. The listed applicant is Lifecore Biomedical, Inc.. The 510(k) number is K032495.

When did THE LIFECORE STAGE-1 ANGLED ABUTMENT SYSTEM receive FDA 510(k) clearance?

THE LIFECORE STAGE-1 ANGLED ABUTMENT SYSTEM received FDA 510(k) clearance on 2003-09-17, under 510(k) number K032495.

Who is the listed applicant for THE LIFECORE STAGE-1 ANGLED ABUTMENT SYSTEM?

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

What is the FDA product code for THE LIFECORE STAGE-1 ANGLED ABUTMENT SYSTEM?

The FDA product code for THE LIFECORE STAGE-1 ANGLED ABUTMENT SYSTEM is DZE.

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Related Devices (Code: DZE)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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