Medtech Insight is part of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC’s registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 8860726.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By

UsernamePublicRestriction
UsernamePublicRestriction

510(k) approval for General Surgical Innovations' dissector / expander device:

This article was originally published in Clinica

Executive Summary

The FDA has cleared General Surgical Innovations' dissector/expander device. The product combines the properties of a balloon dissector and a traditional tissue expander, allowing the surgeon to dissect a space and remotely deploy a tissue expander through the incision in one step. This eliminates the delays caused by the healing process associated with traditional tissue expanders.

Advertisement

Topics

Advertisement
UsernamePublicRestriction

Register

MT086792

Ask The Analyst

Please Note: You can also Click below Link for Ask the Analyst
Ask The Analyst

Your question has been successfully sent to the email address below and we will get back as soon as possible. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts

Cancel