SECURMARK BIOPSY SITE IDENTIFICATION SYSTEM— 510(k) K072913

Substantially Equivalent

Suros Surgical Systems, Inc. A Hologic Company

FDA 510(k) clearance K072913 for SECURMARK BIOPSY SITE IDENTIFICATION SYSTEM, Substantially Equivalent on 2008-01-04. Applicant: Suros Surgical Systems, Inc. A Hologic Company.

Clearance details

Applicant: Suros Surgical Systems, Inc. A Hologic Company
Product code: Code NEU
Advisory panel: General, Plastic Surgery
Date received: 2007-10-12
Decision date: 2008-01-04
Decision: Substantially Equivalent
Clearance type: Special
Location: Indianapolis, IN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code NEU

product code NEU

Injury: 824
Total: 824

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.