X-TIP INTRAOSSEOUS PERFORATOR— 510(k) K990511

Substantially Equivalent

Schiff & Co.

FDA 510(k) clearance K990511 for X-TIP INTRAOSSEOUS PERFORATOR, Substantially Equivalent on 1999-04-27. Applicant: Schiff & Co..

Clearance details

Applicant: Schiff & Co.
Product code: Code DZM
Advisory panel: Dental
Date received: 1999-02-18
Decision date: 1999-04-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Cadwell, NJ, US

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Adverse events under product code DZM

product code DZM

Injury: 139
Total: 139

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.