MEDPOR

Device typePolyethylene craniofacial tissue reconstructive material: A sterile implantable device intended to support, contour, and provide structure for the craniofacial anatomy (i.e., head and face including the chin, cheeks, nose, eye sockets and ears) during reconstructive and plastic surgery procedures. It is typically a high-density polyethylene (PE) material with an interconnecting pore structure that supports tissue ingrowth. The device is available in blocks, sheets, wedges and spheres that can be cut by the surgeon to meet the patient's specific needs. This is a single-use device.

FDA categoryIMPLANT, TEMPORAL

Device ID07613252508670

Catalog number92-9864

AvailabilityPrescription

Single useYes

SterileYes

MRI safetyLabeling does not contain MRI Safety Information

SizeThickness: 2.0 Millimeter

Height49.0 Millimeter

Length46.0 Millimeter