BARD SPERMA-TEX PRESHAPED MESH (2.4X5.6), MODEL 0114700— 510(k) K991637

Name: FDA 510(k) clearance K991637
Creator: U.S. Food and Drug Administration
Published: 1999-06-22

Substantially Equivalent

Davol Inc., Sub. C. R. Bard, Inc.

FDA 510(k) clearance K991637 for BARD SPERMA-TEX PRESHAPED MESH (2.4X5.6), MODEL 0114700, Substantially Equivalent on 1999-06-22. Applicant: Davol Inc., Sub. C. R. Bard, Inc.. Device class: 2.

Clearance details

Applicant: Davol Inc., Sub. C. R. Bard, Inc.
Product code: Code FTL
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 1999-05-12
Decision date: 1999-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Canston, RI, US

Download summary PDF View on FDA.gov ↗

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K081010 — BARD 3DMAX MESH2008-10-07
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Adverse events under product code FTL

product code FTL

Death: 317
Injury: 66,072
Malfunction: 1,273
Other: 3
Total: 67,665

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.