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FDA 510(k)

LOCATOR IMPLANT ANCHOR ATTACHMENT SYSTEM

K-Number: K083324 · 2009-02-25

ApplicantZest Anchors, Inc.
Decision Date2009-02-25
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LOCATOR IMPLANT ANCHOR ATTACHMENT SYSTEM 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 2009-02-25 under 510(k) number K083324. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOCATOR IMPLANT ANCHOR ATTACHMENT SYSTEM?

LOCATOR IMPLANT ANCHOR ATTACHMENT SYSTEM is a medical device that received FDA 510(k) clearance on 2009-02-25. The listed applicant is Zest Anchors, Inc.. The 510(k) number is K083324.

When did LOCATOR IMPLANT ANCHOR ATTACHMENT SYSTEM receive FDA 510(k) clearance?

LOCATOR IMPLANT ANCHOR ATTACHMENT SYSTEM received FDA 510(k) clearance on 2009-02-25, under 510(k) number K083324.

Who is the listed applicant for LOCATOR IMPLANT ANCHOR ATTACHMENT SYSTEM?

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 IMPLANT ANCHOR ATTACHMENT SYSTEM?

The FDA product code for LOCATOR IMPLANT ANCHOR ATTACHMENT SYSTEM is NHA.

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Other records listing Zest Anchors, Inc. 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.

K072878MODIFICATION TO: LOCATOR IMPLANT ANCHORK042466X-2 IMPLANT ABUTMENT; BAR MALE; DISTAL EXTENSION MALEK033699LOCATOR BAR FEMALE, LOCATOR LASER BAR FEMALE, LOCATOR BAR CAST-TO FEMALE, MODELS 08587, 08588, 08586K994257LOCATOR IMPLANT ANCHORK925849ZEST IMPLANT ANCHORK934668ZEST IMPLANT ANCHOR ADVANCED GENERATION (DENTAL)

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Related Devices (Code: NHA)

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.

K262207Cemented Plus AbutmentUnidental Co., Ltd.K260940BellaTek BarsZimVie US Corp, LLCK253999Universal Base ASC Engaging; Universal Base ASC Non-Engaging; Universal Base MUA ASC; Temporary Abutment Engaging and Non-Engaging; Healing Abutment Conical Connection; Omnigrip Clinical Screw Titanium; Omnigrip Prosthetic ScrewNobel Biocare ABK261147Neodent Implant System - NeoConvert FitJJGC Indústria e Comércio de Materiais Dentários S.A.K261122MIST ICImagine Milling Technologies, LLCK260061BioHorizons CEREC Compatible Ti-BasesBioHorizons Implant Systems, 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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