NUVASIVE SURGICAL MESH SYSTEM— 510(k) K081377

Name: FDA 510(k) clearance K081377
Creator: U.S. Food and Drug Administration
Published: 2009-01-15

Substantially Equivalent

Nuvasive, Inc.

FDA 510(k) clearance K081377 for NUVASIVE SURGICAL MESH SYSTEM, Substantially Equivalent on 2009-01-15. Applicant: Nuvasive, Inc.. Device class: 2.

Clearance details

Applicant: Nuvasive, Inc.
Product code: Code FTL
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 2008-05-16
Decision date: 2009-01-15
Decision: Substantially Equivalent
Clearance type: Special
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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K250869 — Parietene Macroporous Mesh (PPM5050 )2025-04-23

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K211757 — Simplify Disc2021-08-20
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K141665 — NuVasive CoRoent System2015-03-13

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.