MODULAR INSTRUMENT SYSTEM FOR MINIMAL INVASIVE SURGERY— 510(k) K990372

Substantially Equivalent

Dr. Fritz GmbH

FDA 510(k) clearance K990372 for MODULAR INSTRUMENT SYSTEM FOR MINIMAL INVASIVE SURGERY, Substantially Equivalent on 1999-10-14. Applicant: Dr. Fritz GmbH.

Clearance details

Applicant: Dr. Fritz GmbH
Product code: Code HET
Advisory panel: Obstetrics/Gynecology
Date received: 1999-02-08
Decision date: 1999-10-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Baldwin Park, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code HET

product code HET

Malfunction: 10,504
Total: 10,504

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.