Orthopaedics Acetabular Wedge Augment System Stryker Hips. Implant with confidence.
Restoration Acetabular Wedge Augment System Restoration Acetabular Wedge Augments, united with Tritanium, Trident, MDM and X3 technologies, is an evolutionary advantage in Total Hip Arthroplasty Advanced Fixation Versatility Simplicity Design Rationale Material The Restoration Acetabular Wedge Augments are manufactured from patented Tritanium 1 Advanced Fixation Technology. Tritanium is created using commercially pure Titanium (CPTi) a biologically compatible material. The Titanium matrix, resulting in a porous bulk foam structure, closely resembles trabecular bone (Figure 1). 2 Wedge Augment material characteristics include: Average Porosity: 63% 3 Coefficient of friction: 1.01 4 Restoration Acetabular Wedge Augments are designed to aid in the reconstruction of minimal to severe bone defects. They provide intraoperative flexibility through optimized screw placement and versatile implant sizing and positioning. Advanced Fixation Tritanium Porous Technology, optimized screw placement Versatility Broad range of implant sizes, adaptable implant geometry and orientation for various defects Simplicity Minimal bone removal, simplified trial to implant placement, intuitive and streamlined instrumentation Figure 1: Magnified view of Tritanium matrix Ancillary Fixation Each Wedge Augment is designed to optimize the number of screw hole options and screw placement to provide enhanced initial stability of the augment. 5 Each screw hole allows for a varying degree of angulation, up to 18, to help achieve purchase with good bone. Either GAP (2080-00XX) or Osteolock (5260-5-0XX) 6.5mm screws can be used to obtain rigid fixation of the Wedge Augment against host bone.
Final Construct Instrumentation Ease of Use The Restoration Wedge Augment instruments, encompassed in a single tray, are simple and easy to use for trialing and implantation. The system is streamlined to include Wedge Augment Trials and a small number of Core Instruments for procedural simplification. The Wedge Augment Trials mimic the geometry of the implants and are color-coded according to OD size. Each trial has the same screw hole configuration as the implant to serve as a visual aid for the location of screws. Simplified Placement The Restoration Acetabular Augment system was designed with provisions for Kirschner Wires (K-wires) to simplify the placement of the trials and to help the surgeon replicate trial positioning with the implant. 66mm OD 62mm OD 58mm OD Use of K-wires to place Restoration Acetabular Wedge Augment 54mm OD 50mm OD 46mm OD Restoration Acetabular Wedge Augment Trials
Wedge Features Tritanium bulk foam Range of OD sizes and thickness for spectrum of defects Optimized screw holes K-Wire holes for simplified placement Product Specifications The Wedge Augments are offered in 18 different sizes consisting of six outer diameter (OD) sizes. The OD sizes range from 46mm to 66mm in 4mm increments. The corresponding inner diameter (ID) for each size is 2mm larger than the OD. For each wedge augment, there are three thickness options. See Table 1. Restoration Acetabular Wedge Augment Table 1 Restoration Acetabular Wedge Augment Specifications Outer Inner No. of Diameter Diameter Thickness Screw Catalog # (mm) (mm) (mm) Holes 5096-4615 46 48 15 3 5096-4620 46 48 20 4 5096-4625 46 48 25 4 5096-5015 50 52 15 3 5096-5020 50 52 20 4 5096-5025 50 52 25 4 5096-5415 54 56 15 4 5096-5420 54 56 20 6 5096-5425 54 56 25 6 5096-5815 58 60 15 6 5096-5820 58 60 20 6 5096-5825 58 60 25 6 5096-6215 62 64 15 6 5096-6220 62 64 20 8 5096-6225 62 64 25 8 5096-6615 66 68 15 6 5096-6620 66 68 20 8 5096-6625 66 68 25 8 Optimized screw hole placement Restoration Modular Conical Distal Stem Tritanium Advanced Fixation Technology Up to 18 of angulation Restoration Modular Cone Body K-wire Holes 18 Wedge Sizes in 3 Thicknesses
Advanced Bearing Options MDM X3 The MDM X3 Mobile Bearing Hip System is the latest addition to Stryker s comprehensive solution for both primary and revision total hip arthroplasty (THA). MDM X3 is designed to address stability, 6 implant longevity 7 and advanced fixation helping orthopaedic surgeons with a wide breadth of reconstruction challenges they may face in hip surgeries. Tritanium, Trident and X3 Tritanium Advanced Fixation Technology, developed from commercially pure Titanium (CPTi) a biologically compatible material, is applied to Stryker s Multi-Hole shell to aid in revision THA. Trident, an evolutionary shell design with over 10 years of clinical history, has demonstrated the lowest revision rate (2.4%) among cementless cups at five years according to the 2010 National Joint Registry of England and Wales. 8 Both the Tritanium and Trident Acetabular Systems feature a patented 15 locking mechanism that outperforms competitive designs in laboratory testing, 9 and is designed to minimize backside wear 9 and maximize jump distance for increased stability. 10 Compatible with X3 Advanced Bearing Technology, Tritanium and Trident provide solutions for the range of hip surgeries. Advanced Femoral Options Restoration Modular The Restoration Modular Stem System is designed to allow surgeons to independently achieve the main goals of hip surgery attain solid fixation and restore hip biomechanics, 12 all with a straightforward set of instrumentation. Versatility System addresses femoral Type 1 through Type 4 revisions 13,14 Stability Designed to allow for restoration of proper biomechanics through independent adjustment of leg length, offset and version 12 Simplicity Simple, straightforward instrumentation to allow for OR efficiency The Restoration Modular Stem System The Power of X3 The patented 16 X3 Advanced Bearing Technology is designed to minimize the risk of wear and consequently help prolong the life of the implant. 7,11 X3 has demonstrated a 97% reduction in wear compared to conventional polyethylene. 11
References 1. US Patent #7,458,991, 7,740,795, 7,674,426. 2. Ricci J. L., Kauffman J., Jaffe W., et al., Comparison of Osseointegration and Bone Adhesion to Commercially Pure Titanium and Titanium Alloy, 23rd Ann. Mtg. Society for Biomaterials, 1997. 3. Stryker Test Report RD-10-044 4. Stryker Test Report RD-07-077 5. Stryker Test Report RD-10-050 6. Heffernan, C., Bhimji, S., Macintyre, J., et al. (2011). Development and Validation of a Novel Modular Dual Mobility Hip Bearing. ORS Annual Meeting Poster #1165. 7. Herrera, L., Lee, R., Longaray, J., et al. (2010). Edge Loading Wear due to Inclination Angle for Three Contemporary Hip Bearings. 56th Annual ORS Meeting. Poster #2259. 8. The National Joint Registry of England and Wales, Annual Report 2010. Table 3.3. Based on revision rates according to cup brands for primary hip replacement procedures, undertaken between 1st April 2003 and 31st December 2009, which were linked to a HES/PEDW episode. 9. Litsky, AS, et al., Micromotion between the Cup and the Liner in Modular Acetabular Prostheses, 1999 Society for Biomaterials, 25th Annual Meeting Transactions. 10. Nevelos, J., Bhimji, S., Macintyre, J., et al. (2010). Acetabular Bearing Design has a Greater Influence on Jump Distance than Head Size. 56th Annual ORS Meeting: Poster #2028. 11. Stryker Orthopaedics Restoration ADM X3 28 mm ID acetabular inserts made of X3 Gas Plasma Sterilized UHMWPE, show a 97% reduction in volumetric wear rate versus 28 mm ID Restoration ADM Duration Gamma Radiation Sterilized UHMWPE. Both ADM constructs utilized a 54mm OD shell and the inserts were approximately 9.9 mm thick. Testing was conducted under multi-axial hip joint simulation for 5 million cycles using a 28mm CoCr modular femoral head articulating counterface and calf serum lubricant. Volumetric wear rates were 109.7±6.0 mm 3 /10 6 cycles and -1.03 ± 3.8 mm 3 /10 6 cycles for Duration and X3 polyethylene insert test samples. Although in-vitro hip wear simulation methods have not been shown to quantitatively predict clinical wear performance, the current model has been able to reproduce correct wear resistance rankings for some materials with documented clinical results. 1-3 [1] Wang, A, et. al., Tribology International, Vol. 31, No. 1-3: 17-33, 1998. [2] Essner, A. et. al., 44th Annual Meeting, ORS, New Orleans, Mar. 16-19, 1998: 774. [3] Essner, A. et. al., 47th Annual Meeting, ORS, San Francisco, Feb. 25-28, 2001: 1007. 12. Goldberg G, Hozack WJ. Modular Stems for Revision of Peri-prosthetic Hip Fractures: Indications and Technique. Seminars in Arthroplasty 2006 17: 15-17. 13. Patel PD, Klika AK, Murray TG, Elsharkawy KA, Krebs VE, Barsoum WK. Influence of Technique With distally fixed Modular Stems in Revision Total Hip Arthroplasty. Journal of Arthroplasty 2010. 25: 926-931. 14. Holt G, McCaul J, Jones B, Ingram R, Stark A. Outcome After Femoral Revision Using the Restoration Cone / Conical Femoral Revision Stem. OrthoSuperSite. January 2011. 15. US Patent # 6,475,243. 16. US Patents # 7,517,919, 7,714,036. Joint Replacements Trauma, Extremities & Deformities Craniomaxillofacial Spine Biologics Surgical Products Neuro & ENT Interventional Spine Navigation Endoscopy Communications Imaging Patient Care & Handling Equipment EMS Equipment 325 Corporate Drive Mahwah, NJ 07430 t: 201 831 5000 www.stryker.com A surgeon must always rely on his or her own professional clinical judgment when deciding whether to use a particular product when treating a particular patient. Stryker does not dispense medical advice and recommends that surgeons be trained in the use of any particular product before using it in surgery. The information presented is intended to demonstrate the breadth of Stryker product offerings. A surgeon must always refer to the package insert, product label and/or instructions for use before using any Stryker product. Products may not be available in all markets because product availability is subject to the regulatory and/or medical practices in individual markets. Please contact your Stryker representative if you have questions about the availability of Stryker products in your area. Stryker Corporation or its divisions or other corporate affiliated entities own, use or have applied for the following trademarks or service marks: MDM, Osteolock, Restoration, Stryker, Trident, Tritanium, X3. All other trademarks are trademarks of their respective owners or holders. Literature Number: LRWS-B KAM/GS 8/11 165 Copyright 2011 Stryker Printed in USA.