<tt id="awzwg"><noscript id="awzwg"></noscript></tt>

  • <cite id="awzwg"></cite>

    1. <source id="awzwg"><nav id="awzwg"></nav></source>
      1. <video id="awzwg"></video>
      2. Arcos? Modular Femoral Revision System

        1000x1000_insetimage_Hips_Arcos

        Zimmer Biomet’s Arcos Modular Femoral Revision System meets the demands of complex hip revision surgery by offering surgeons and OR staff the ability to customize both the hip implant and its corresponding instruments. Three proximal and five distal geometry options provide surgeons 117 proximal/distal combinations and multiple auxiliary fixation options for various femoral defects. This allows surgeons and OR staff the surgical control, customization options, and reproducibility to efficiently address both patient and practice needs.

        The features of the Arcos Modular Femoral Revision System include:

        • Three proximal body options:
          • Cone
          • Broach
          • Calcar
        • Five distal stem options:
          • STSTM (Splined Tapered Stem)
          • Slotted
          • Bullet-tip
          • Interlocking
          • ETO (Extended Trochanteric Osteotomy)
        • Multiple surgical technique options
          • Ream-over
          • Sterile field
          • In-femur
        • One simple, easy to use instrumentation platform
        • Standard and high offset options reproduce various patient anatomies without lengthening the leg
        • Consistent sizing (1mm increments) for increased O.R. efficiency and accurate matching of the patient’s femur
        • Roller-hardened taper junction technology for greater fatigue strength and three times more strength in cantilever beam testing than non-roller hardened tapers1
        • Clinically proven PPS? coating allows for initial scratch-fit stability and biologic fixation2-9
        • Flexibility of titanium allows for stress transfer to preserve cortical density10

        Providing Options for Intraoperative Flexibility

        In femoral revisions, it is necessary to address metaphyseal and diaphyseal deficiencies independently. With three proximal bodies and five distal stems, which all work together regardless of size, a surgeon is able to address deficiencies in both regions of the femur independent of each other. This compatibility allows for a surgeon to change stems intraoperatively if encountered with something different from their preoperative planning. The availability of standard and high offset proximal body offerings are additional tools that allow the surgeon intraoperative flexibility to address patient needs as they arise.

        ?

        Bolt and Claw Auxiliary Option

        The Arcos Modular Femoral Revision System has the ability to use auxiliary implants to reattach the trochanteric fragment directly to the implant. By reattaching the trochanteric fragment in this fashion, the soft tissue and bony fragment are stabilized and provide an additional level of stability.

        ?

        Streamlined Instrumentation

        Designed with common proximal implant and instrument geometries, the Arcos Platform design allows for intraoperative revision efficiency by reducing the number of instrument cases required to a number comparable to a primary hip surgery.

        arcos-1

        Common Implant and Instrument Geometry

        arcos-2
        • PPS? Porous Plasma Spray

        ?

        Additional Information

        Surgical Techniques

        1. Data on file at Biomet. Bench test results not necessarily indicative of clinical performance.
        2. Hozack, W. et al. Primary Cementless Hip Arthroplasty with a Titanium Plasma Sprayed Prosthesis. Clinical Orthopaedics and Related Research. 333: 217-25, 1996.
        3. Head, W. et al. A Titanium Cementless Calcar Replacement Prosthesis in Revision Surgery of the Femur: 13 Year Experience. Journal of Arthroplasty. 16(8): 183-7, 2001.
        4. Head, W. et al. The Proximal Porous Coating Alternative for Primary Arthroplasty. Orthopedics. 22(9): 813-5, 1999.
        5. Keisu, K. et al. Primary Cementless Total Hip Arthroplasty in Octogenarians: Two to Eleven Year Follow-up. Journal of Bone and Joint Surgery. 83: 359, 2001.
        6. McLaughlin, J. et al. Total Hip Arthroplasty in Young Patients. 8 to 13 Year Results Using an Uncemented Stem. Clinical Orthopaedics and Related Research. 373: 152-63, 2000.
        7. Parvizi, J. et al. Prospective Matched-Pair Analysis of Hydroxyapatite-Coated and Uncoated Femoral Stems in Total Hip Arthroplasty. Journal of Bone and Joint Surgery. 83: 783-6, 2004.
        8. McLaughlin, J. et al. Total Hip Arthroplasty with an Uncemented Femoral Component. A Long Term study of the Taperloc Stem. Journal of Arthroplasty. 19(2): 151-6, 2004.
        9. Meding, K. et al. Minimum Ten-Year Follow-up of a Straight-Stemmed, Plasma-Sprayed, Titanium-Alloy, Uncemented Femoral Component in Primary Total Hip Arthroplasty. Journal of Bone and Joint Surgery. 86: 92-7, 2004
        10. Musgrave, D. et al. Effects of Coronally Slotted Femoral Prosthesis on Cortical bone Strain. Journal of Arthroplasty. 12(6): 657-69, 1997.

        Instrumentation should not limit surgeons’ implant selection or preferred surgical technique. Zimmer Biomet’s Arcos? Modular Femoral Revision System is designed to provide the option to use any implant combination with the surgical technique that is required to address each patient’s needs.

        Designed with common proximal implant and instrument geometries, the Arcos platform design allows for intraoperative revision efficiency by reducing the number of instrument cases required to a number comparable to a primary hip surgery.?

        ?

        Legal Manufacturer:??????????????????????

        Biomet Orthopedics
        56 East Bell Drive
        P.O. Box 587
        Warsaw, Indiana 46581 USA


        All content herein is protected by copyright, trademarks and other intellectual property rights, as applicable, owned by or licensed to Zimmer Biomet or its affiliates unless otherwise indicated, and must not be redistributed, duplicated or disclosed, in whole or in part, without the express written consent of Zimmer Biomet. ?
        This material is intended for health care professionals. ?Distribution to any other recipient is prohibited.
        For product information, including indications, contraindications, warnings, precautions, potential adverse effects and patient counseling information, see the package insert and information on this website. To obtain a copy of the current Instructions for Use (IFU) for full prescribing and risk information, please call 1-800-348-2759, press 4 for 411 Technical Support.
        青春在线草免费视频