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Precision Spine Gets FDA 510k Marketing Clearance

Wednesday, December 12, 2012 5:01:00 AM PDT | VentureDeal
   Parsippany, New Jersey  --  Medical device company Precision Spine says that it has received 510(k) marketing clearance from the FDA for its minimally invasive spinal access system.

The Mini-Max Minimally Invasive Access System promises to enable spine surgeons to perform minimally invasive procedures in improved manner.

The company says that the system uses techniques that are already familiar to surgeons and facilitate "greater direct visualization of the spine."

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