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FDA permits marketing of a new device for abdominal surgery
date:May 04, 2012
urgeons to assemble and disassemble the device inside the abdomen, device failures and risks, and how to address risks.
The device is indicated for use for abdominal surgery only. Risks associated with the device include device failure, user error, abdominal cavity damage, infection, and tissue inflammation.
The Percutaneous Surgical Set is manufactured by Cincinnatibased Ethicon Endo-Surgery Inc., a subsidiary of the Johnson Johnson Co.

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