Profile: Mako Surgical Corp. offers MAKOplasty®, Rio®robotic arm interactive orthopedic system, Restoris® family of knee implant systems. Our MAKOplasty® is a restorative surgical solution that enables orthopedic surgeons to treat patient-specific, early to mid-stage osteoarthritic knee disease with consistent reproducible precision using the Rio® robotic arm interactive orthopedic system. Our Rio® assists the surgeon in achieving natural knee kinematics. It enables pre-resection capture of patient-specific kinematic tracking through full flexion and extension. Our Restoris® has uniquely designed implant components for true anatomic resurfacing. It is targeted to resurface the patient-specific disease state .
The company has ~130 employees. NASDAQ:MAKO (SEC Filings)
FDA Registration Number: 3005985723
7 Products/Services (Click for related suppliers)
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| • Knee Joint Femorotibial Metal/Polymer Non-constrained Cemented Prosthesis (FDA Code: HSX / 888.3520) A knee joint femorotibial metal/polymer non-constrained cemented prosthesis is a device intended to be implanted to replace part of a knee joint. The device limits minimally (less than normal anatomic constraints) translation in one or more planes. It has no linkage across-the-joint. This generic type of device includes prostheses that have a femoral condylar resurfacing component or components made of alloys, such as cobalt-chromium-molybdenum, and a tibial component or components made of ultra-high molecular weight polyethylene and are intended for use with bone cement (888.3027). |
| • Neurological Stereotaxic Instrument (FDA Code: HAW / 882.4560) A stereotaxic instrument is a device consisting of a rigid frame with a calibrated guide mechanism for precisely positioning probes or other devices within a patient's brain, spinal cord, or other part of the nervous system. |
| • Partial Knee Resurfacing |
| • Polymer/Metal/Polymer Cemented Semi-Constrained Partial Knee Patellofemorotibial Prosthesis (FDA Code: NPJ / 888.3560) A knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis is a device intended to be implanted to replace a knee joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across-the-joint. This generic type of device includes prostheses that have a femoral component made of alloys, such as cobalt-chromium-molybdenum, and a tibial component or components and a retropatellar resurfacing component made of ultra-high molecular weight polyethylene. This generic type of device is limited to those prostheses intended for use with bone cement (888.3027). |
| • Robotic Arm Interactive Orthopedic Systems |
| • Semi-Constrained Femorotibial Knee Prosthesis (FDA Code: HRY / 888.3530) A knee joint femorotibial metal/polymer semi-constrained cemented prosthesis is a device intended to be implanted to replace part of a knee joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across-the-joint. This generic type of device includes prostheses that consist of a femoral component made of alloys, such as cobalt-chromium-molybdenum, and a tibial component made of ultra-high molecular weight polyethylene and is limited to those prostheses intended for use with bone cement (888.3027). |
| • Semi-Constrained Patellofemoral Knee Prosthesis (FDA Code: KRR / 888.3540) A knee joint patellofemoral polymer/metal semi-constrained cemented prosthesis is a two-part device intended to be implanted to replace part of a knee joint in the treatment of primary patellofemoral arthritis or chondromalacia. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across-the-joint. This generic type of device includes a component made of alloys, such as cobalt-chromium-molybdenum or austenitic steel, for resurfacing the intercondylar groove (femoral sulcus) on the anterior aspect of the distal femur, and a patellar component made of ultra-high molecular weight polyethylene. This generic type of device is limited to those devices intended for use with bone cement (888.3027). The patellar component is designed to be implanted only with its femoral component. |