ORTHO ANCHOR SCREWS— 510(k) K073461

Substantially Equivalent

Mis Implants Technologies , Ltd.

FDA 510(k) clearance K073461 for ORTHO ANCHOR SCREWS, Substantially Equivalent on 2008-01-25. Applicant: Mis Implants Technologies , Ltd..

Clearance details

Applicant: Mis Implants Technologies , Ltd.
Product code: Code OAT
Advisory panel: Dental
Date received: 2007-12-10
Decision date: 2008-01-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shlomi, IL

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Adverse events under product code OAT

product code OAT

Injury: 355
Total: 355

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.