FDA 510(k)

LOCATOR BAR FEMALE, LOCATOR LASER BAR FEMALE, LOCATOR BAR CAST-TO FEMALE, MODELS 08587, 08588, 08586

K-Number: K033699 · 2004-04-22

Decision Date2004-04-22

Product CodeDZE

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

LOCATOR BAR FEMALE, LOCATOR LASER BAR FEMALE, LOCATOR BAR CAST-TO FEMALE, MODELS 08587, 08588, 08586 is the device name listed in this FDA 510(k) record. The listed applicant is Zest Anchors, Inc.. It received FDA 510(k) clearance on 2004-04-22 under 510(k) number K033699. 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 LOCATOR BAR FEMALE, LOCATOR LASER BAR FEMALE, LOCATOR BAR CAST-TO FEMALE, MODELS 08587, 08588, 08586?

LOCATOR BAR FEMALE, LOCATOR LASER BAR FEMALE, LOCATOR BAR CAST-TO FEMALE, MODELS 08587, 08588, 08586 is a medical device that received FDA 510(k) clearance on 2004-04-22. The listed applicant is Zest Anchors, Inc.. The 510(k) number is K033699.

When did LOCATOR BAR FEMALE, LOCATOR LASER BAR FEMALE, LOCATOR BAR CAST-TO FEMALE, MODELS 08587, 08588, 08586 receive FDA 510(k) clearance?

LOCATOR BAR FEMALE, LOCATOR LASER BAR FEMALE, LOCATOR BAR CAST-TO FEMALE, MODELS 08587, 08588, 08586 received FDA 510(k) clearance on 2004-04-22, under 510(k) number K033699.

Who is the listed applicant for LOCATOR BAR FEMALE, LOCATOR LASER BAR FEMALE, LOCATOR BAR CAST-TO FEMALE, MODELS 08587, 08588, 08586?

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

What is the FDA product code for LOCATOR BAR FEMALE, LOCATOR LASER BAR FEMALE, LOCATOR BAR CAST-TO FEMALE, MODELS 08587, 08588, 08586?

The FDA product code for LOCATOR BAR FEMALE, LOCATOR LASER BAR FEMALE, LOCATOR BAR CAST-TO FEMALE, MODELS 08587, 08588, 08586 is DZE.

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Other records listing Zest Anchors, Inc. as applicant

K083324LOCATOR IMPLANT ANCHOR ATTACHMENT SYSTEM K072878MODIFICATION TO: LOCATOR IMPLANT ANCHOR K042466X-2 IMPLANT ABUTMENT; BAR MALE; DISTAL EXTENSION MALE K994257LOCATOR IMPLANT ANCHOR K925849ZEST IMPLANT ANCHOR K934668ZEST IMPLANT ANCHOR ADVANCED GENERATION (DENTAL)

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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.