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FDA 510(k)

ZEUS MICROWRIST ROBOTIC SURGICAL SYSTEM

K-Number: K013551 · 2002-03-28

ApplicantComputer Motion, Inc.
Decision Date2002-03-28
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ZEUS MICROWRIST ROBOTIC SURGICAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Computer Motion, Inc.. It received FDA 510(k) clearance on 2002-03-28 under 510(k) number K013551. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZEUS MICROWRIST ROBOTIC SURGICAL SYSTEM?

ZEUS MICROWRIST ROBOTIC SURGICAL SYSTEM is a medical device that received FDA 510(k) clearance on 2002-03-28. The listed applicant is Computer Motion, Inc.. The 510(k) number is K013551.

When did ZEUS MICROWRIST ROBOTIC SURGICAL SYSTEM receive FDA 510(k) clearance?

ZEUS MICROWRIST ROBOTIC SURGICAL SYSTEM received FDA 510(k) clearance on 2002-03-28, under 510(k) number K013551.

Who is the listed applicant for ZEUS MICROWRIST ROBOTIC SURGICAL SYSTEM?

The FDA 510(k) record lists Computer Motion, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ZEUS MICROWRIST ROBOTIC SURGICAL SYSTEM?

The FDA product code for ZEUS MICROWRIST ROBOTIC SURGICAL SYSTEM is GCJ.

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Other records listing Computer Motion, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K031956MODIFICATION TO HERMES O.R. CONTROL CENTERK031720MODIFICATION TO HERMES O.R. CONTROL CENTERK031382MODIFICATION TO HERMES O.R. CONTROL CENTERK030578BIPOLAR GRASPER AND BIPOLAR SCISSORS FOR THE ZEUS MICROWRIST SURGICAL SYSTEMK030718SCB COMPUTER MOTION INTERFACE CONTROLLERK030240MODIFICATION TO HERMES OPERATING ROOM CONTROL CENTER

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Related Devices (Code: GCJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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