Details
Device typeOrthopaedic cement, non-antimicrobial: A substance designed to be used in arthroplastic and/or osteosynthetic procedures for the fixation of polymer or metallic implants to the living bone. It may also be intended for use as a filler in the case of bone pathologies (e.g., to stabilize and reinforce vertebral body structures in vertebroplasty and kyphoplasty). It is typically made from methylmethacrylate, polymethylmethacrylate (PMMA), esters of methacrylic acid or copolymers containing polymethylmethacrylate and polystyrene. This device does not contain an antimicrobial agent. After application, this device cannot be reused.
FDA categoryCement, Bone, Vertebroplasty
Device ID00815212021404
Catalog numberG80005
Single useYes
SterileYes
MRI safetyLabeling does not contain MRI Safety Information