LRTM SURGICAL MESH— 510(k) K070560

Name: FDA 510(k) clearance K070560
Creator: U.S. Food and Drug Administration
Published: 2007-06-11

Substantially Equivalent

Lifecell Corp.

FDA 510(k) clearance K070560 for LRTM SURGICAL MESH, Substantially Equivalent on 2007-06-11. Applicant: Lifecell Corp.. Device class: 2.

Clearance details

Applicant: Lifecell Corp.
Product code: Code FTM
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 2007-02-27
Decision date: 2007-06-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Branchburg, NJ, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code FTM

product code FTM

Death: 17
Injury: 2,174
Total: 2,191

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.