PILLAR NASAL, DORSAL COLUMELLA AND NASAL DORSUM IMPLANTS— 510(k) K992242

Substantially Equivalent

Pillar Surgical, Inc.

FDA 510(k) clearance K992242 for PILLAR NASAL, DORSAL COLUMELLA AND NASAL DORSUM IMPLANTS, Substantially Equivalent on 1999-11-22. Applicant: Pillar Surgical, Inc..

Clearance details

Applicant: Pillar Surgical, Inc.
Product code: Code FZE
Advisory panel: General, Plastic Surgery
Date received: 1999-07-02
Decision date: 1999-11-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: La Jolla, CA, US

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Adverse events under product code FZE

product code FZE

Injury: 138
Total: 138

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.