Device typeOrthopaedic implant impactor, reusable: A non-powered, hand-held, surgical instrument designed to transmit impact forces, typically from a hammer/mallet to an orthopaedic implant (e.g., intramedullary nail or stem), to position/drive the implant into the body during impact-based implantation. It commonly includes an impact-absorbing handle with a distal end shaped to conform to the implant (i.e., flat or anatomically curved). This is a reusable device.
FDA categoryHip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented, Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented, Hip, semi-constrained, cemented, metal/polymer + additive, cemented, Prosthesis, hip, constrained, cemented or uncemented, metal/polymer, prosthesis, hip, constrained, cemented or uncemented, metal/polymer, + additive, Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented, Prosthesis, hip, semi-constrained, metal/polymer, cemented, PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED, TISSUE GRAFT OF LESS THAN 6MM
Device ID00880304926868
Catalog number010002726
AvailabilityPrescription
MRI safetyLabeling does not contain MRI Safety Information