FDA Product Code MMX: Device, Percutaneous Retrieval

Under FDA product code MMX, percutaneous retrieval devices are cleared for the endovascular retrieval of foreign bodies and misplaced objects from the cardiovascular system.

These snare, basket, or grasper devices are delivered through catheters to capture and remove fragmented catheters, guide wires, embolized devices, and other intravascular foreign bodies without open surgery.

MMX devices are Class II medical devices, regulated under 21 CFR 870.5150 and reviewed by the FDA Cardiovascular panel.

Leading manufacturers include Argon Medical Devices, Inc., Abbott Medical and Cook Incorporated.