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

Name: FDA 510(k) clearance K992242
Creator: U.S. Food and Drug Administration
Published: 1999-11-22

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.. Device class: 2.

Clearance details

Applicant: Pillar Surgical, Inc.
Product code: Code FZE
Device class: Class 2
Regulation: 21 CFR 878.3680
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

Download summary PDF View on FDA.gov ↗

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K992239 — PILLAR CHIN IMPLANT1999-11-22
K992240 — PILLAR MALAR IMPLANT1999-11-22

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.