Case Report
Using a Microsurgical Robotic Platform for In-flap Anastomosis in Autologous Bipedicular Breast Reconstruction
Plastic & Reconstructive Surgery – Global Open
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The Symani Surgical System is authorized for use in the U.S. by the FDA and is a CE marked medical device. Symani is manufactured in Pisa, Italy.
Clinical indications vary by geography. Refer to global indications for more information.
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