da Vinci Surgery
 

Clinical Evidence

Since the introduction of the da Vinci System more than ten years ago, the da Vinci System has been used successfully in tens of thousands of procedures. Its safety and efficacy have been documented in hundreds of clinical publications. The literature supporting da Vinci ’s use is extensive, covering all surgical specialties where the System is used.

To the left are links to bibliographies organized by specialty, providing clinical evidence that supports the use of the da Vinci System. Links to abstracts available on the National Library of Medicine’s website are provided for your reference.

For complete, full-text articles:

Within the listing on The National Library of Medicine website, you’ll find links to publishers’ sites, which sell electronic copies. Web-based document delivery services are also available (search for “document delivery services” or “document delivery supplier”) that may help with more complex requests.

Important Safety Information

Serious complications may occur in any surgery, including da Vinci® Surgery, up to and including death. Individual surgical results may vary. Patients should talk to their doctor to decide if da Vinci Surgery is right for them. Patients and doctors should review all available information on non-surgical and surgical options in order to make an informed decision. Please also refer to http://www.daVinciSurgery.com/Safety for Important Safety Information.

When Is Single-Site Technology Used and What Are the Risks?

da Vinci Surgery with Single-Site® Instruments is cleared for use in gallbladder removal, and for hysterectomy and ovary removal for benign conditions. Patients who are not candidates for non-robotic minimally invasive surgery are also not candidates for da Vinci Surgery, including da Vinci Surgery with Single-Site Instruments. There may be an increased risk of incision-site hernia with single-incision surgery, including Single-Site surgery with the da Vinci System. Single-Site® Instruments for the da Vinci® Si System bear the CE mark. This device is cleared for commercial distribution in the U.S. for laparoscopic cholecystectomy, and for hysterectomy and salpingo-oophorectomy for benign conditions.

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* Important Patient Safety Information.