ZEUS MICROWRIST ROBOTIC SURGICAL SYSTEM AND ACCESSORIES— 510(k) K021152

Name: FDA 510(k) clearance K021152
Creator: U.S. Food and Drug Administration
Published: 2002-09-24

Substantially Equivalent

Computer Motion, Inc.

FDA 510(k) clearance K021152 for ZEUS MICROWRIST ROBOTIC SURGICAL SYSTEM AND ACCESSORIES, Substantially Equivalent on 2002-09-24. Applicant: Computer Motion, Inc.. Device class: 2.

Clearance details

Applicant: Computer Motion, Inc.
Product code: Code NAY
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 2002-04-10
Decision date: 2002-09-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Goleta, CA, US

Download summary PDF View on FDA.gov ↗

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K030578 — BIPOLAR GRASPER AND BIPOLAR SCISSORS FOR THE ZEUS MICROWRIST SURGICAL SYSTEM2003-06-24
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Adverse events under product code NAY

product code NAY

Death: 433
Injury: 7,927
Malfunction: 93,790
Other: 19
Total: 102,169

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.