LOCATOR IMPLANT ANCHOR ATTACHMENT SYSTEM— 510(k) K083324

Name: FDA 510(k) clearance K083324
Creator: U.S. Food and Drug Administration
Published: 2009-02-25

Substantially Equivalent

Zest Anchors, Inc.

FDA 510(k) clearance K083324 for LOCATOR IMPLANT ANCHOR ATTACHMENT SYSTEM, Substantially Equivalent on 2009-02-25. Applicant: Zest Anchors, Inc.. Device class: 2.

Clearance details

Applicant: Zest Anchors, Inc.
Product code: Code NHA
Device class: Class 2
Regulation: 21 CFR 872.3630
Advisory panel: Dental
Date received: 2008-11-12
Decision date: 2009-02-25
Decision: Substantially Equivalent
Clearance type: Special
Location: Escondido, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code NHA

product code NHA

Injury: 1,270
Malfunction: 2,860
Total: 4,130

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.