Vertebroplasty Polymeric Modular Pre-Formed Bone Cement Suppliers
EMAIL INQUIRY to 2 suppliers
Benvenue Medical, Inc. | Address: 3052 Bunker Hill Lane, Suite 120, Santa Clara, California 95054, USA 
www.benvenuemedical.com | Send Inquiry | Phone: +1-(408)-4549300
FDA Registration: 3007033608
Products: Medical Devices for Ambulatory Treatment of Spinal Disorders, Lumbar Intervertebral Fusion Device with Bone Graft (FDA Code: MAX), Vertebroplasty Spinal Channeling Instrument (FDA Code: OCJ), Vertebroplasty Polymeric Modular Pre-Formed Bone Cement (FDA Code: OBL), ...
Benvenue Medical, Inc. deals with surgical solutions to treat spinal disorders. We provide Kiva™ vertebral compression fracture treatment system. This system is used in the treatment of osteopor more...
www.benvenuemedical.com | Send Inquiry | Phone: +1-(408)-4549300
FDA Registration: 3007033608
Products: Medical Devices for Ambulatory Treatment of Spinal Disorders, Lumbar Intervertebral Fusion Device with Bone Graft (FDA Code: MAX), Vertebroplasty Spinal Channeling Instrument (FDA Code: OCJ), Vertebroplasty Polymeric Modular Pre-Formed Bone Cement (FDA Code: OBL), ...
Benvenue Medical, Inc. deals with surgical solutions to treat spinal disorders. We provide Kiva™ vertebral compression fracture treatment system. This system is used in the treatment of osteopor more...
Spine Wave, Inc. | Address: Three Enterprise Drive, Suite 210, Shelton, Connecticut 06484, USA
www.spinewave.com | Send Inquiry | Phone: +1-(203)-944-9494, 877-844-4225
FDA Registration: 3004638600
Products: Pedicle Screw System, Vertebral Body Replacement System, Medical Devices, Disposable Aspiration and Injection Needle (FDA Code: GAA), General & Plastic Surgery Surgical Cannula (FDA Code: GEA), Spinal Vertebral Body Replacement Device (FDA Code: MQP), ...
Spine Wave, Inc. deals with the development and delivery of innovative medical devices for the treatment of spinal disorders. Our trade mark products are Spine Wave™, StaXx®, CapSure®, a more...
www.spinewave.com | Send Inquiry | Phone: +1-(203)-944-9494, 877-844-4225
FDA Registration: 3004638600
Products: Pedicle Screw System, Vertebral Body Replacement System, Medical Devices, Disposable Aspiration and Injection Needle (FDA Code: GAA), General & Plastic Surgery Surgical Cannula (FDA Code: GEA), Spinal Vertebral Body Replacement Device (FDA Code: MQP), ...
Spine Wave, Inc. deals with the development and delivery of innovative medical devices for the treatment of spinal disorders. Our trade mark products are Spine Wave™, StaXx®, CapSure®, a more...
EMAIL INQUIRY to 2 Vertebroplasty Polymeric Modular Pre-Formed Bone Cement suppliers
FDA Code / Regulation: OBL / 888.3027
Polymethylmethacrylate (PMMA) bone cement is a device intended to be implanted that is made from methylmethacrylate, polymethylmethacrylate, esters of methacrylic acid, or copolymers containing polymethylmethacrylate and polystyrene. The device is intended for use in arthroplastic procedures of the hip, knee, and other joints for the fixation of polymer or metallic prosthetic implants to living bone.
Classification. Class II (special controls). The special control for this device is the FDA guidance document entitled "Class II Special Controls Guidance Document: Polymethylmethacrylate (PMMA) Bone Cement."
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