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FDA 510(k)

DUAL TOP ANCHOR SYSTEM SCREWS

K-Number: K033767 · 2004-02-24

ApplicantJeil Medical Corporation
Decision Date2004-02-24
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DUAL TOP ANCHOR SYSTEM SCREWS is the device name listed in this FDA 510(k) record. The listed applicant is Jeil Medical Corporation. It received FDA 510(k) clearance on 2004-02-24 under 510(k) number K033767. 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 DUAL TOP ANCHOR SYSTEM SCREWS?

DUAL TOP ANCHOR SYSTEM SCREWS is a medical device that received FDA 510(k) clearance on 2004-02-24. The listed applicant is Jeil Medical Corporation. The 510(k) number is K033767.

When did DUAL TOP ANCHOR SYSTEM SCREWS receive FDA 510(k) clearance?

DUAL TOP ANCHOR SYSTEM SCREWS received FDA 510(k) clearance on 2004-02-24, under 510(k) number K033767.

Who is the listed applicant for DUAL TOP ANCHOR SYSTEM SCREWS?

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

What is the FDA product code for DUAL TOP ANCHOR SYSTEM SCREWS?

The FDA product code for DUAL TOP ANCHOR SYSTEM SCREWS is 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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