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DePuy RECLAIM Design Rationale

dESIGn RATIonALE ReClaiM DePuy Orthopaedics EMEA is a trading division of DePuy International Limited. Registered Office: St. Anthony's Road, Leeds LS11 8DT, England Registered in England No. 3319712 ©DePuy International Ltd. and DePuy Orthopaedics, Inc. 2012 Design Rationale. Approach Patients with CONFIDENCE Limited arranty and Disclaimer DePuy Synthes products are sold with a limited warranty to the original purchaser against defects in workmanship and materials. Any other express or implied warranties, including warranties of merchantability or fitness, are hereby disclaimed.. Design Rationale and Surgical Technique. 2 3 Introduction That is why DePuy Orthopaedics has created GLOBAL UNITE, a next-generation platform system. The modular proximal bodies allow the surgeon to restore joint height in press-fit and cemented applications, while the modular suture collar allows for anatomic reconstruction of the.

DePuy LPS Limb Preservation System - Surgical Technique

design incorporates a wear-resistance zone, so patients may experience a substantial decrease in metal wear debris and ion release when compared to conventional metal-on-metal designs. combined with DePuy TrueGlide™ technology, the aSphere head helps facilitate a more fluid range of natural motion for patients. Optimized Wear-Resistance Zone DePuy Gription TF - Design Rationale/Surgical Technique. DePuy's GRIPTION TF Acetabular Revision System is an innovative technology for addressing bone defects in complex acetabular revision surgery. It represents the latest advances in materials,.. RECLAIM® Modular Revision Hip System Surgical Technique DePuy Synthes Joint Reconstruction 7 105 mm 95 mm 85 mm 75 mm The Clear Out Reamer is designed to obtain clear access for the reamer extension prior to progressive distal reaming Femoral Component Design.CORR235, October 1988: 148-165. 4. Paul, H.A., et al. Development of a Surgical Robot for Cementless Total Hip Arthroplasty. CORR285, Dec. 1992: 57-66. * Additional sizes are available. IMPORTANT: This Essential Product Information sheet does not include all of the information necessary for selection and use of. Design Rationale TRI-LOCK Bone Preservation Stem DePuy Synthes Joint Reconstruction 5 • GRIPTION Porous Coating has a 1.2 coefficient of friction exceeding that of plasma spray and porous tantalum material. 2,

DePuy Synthes J&J Medical Device

LCP Distal Femur / Promixal Lateral Tibia 4Todos los catálogos y folletos técnicos Depuy Synthes

4 DePuy Synthes ESC® Enhanced Stability Liners Design Rationale & Surgical Technique Potential ROM Up to 113˚ Advanced Stability 0 40 80 120 Range of Motion (degrees) 100 60 20 140 DePuy Synthes ESC Liner 1 44 mm 113 Biomet FreedomTM Constrained2 36 mm 110 Smith & Nephew R3 Constrained7 102 DePuy Synthes DURALOC Acetabular Cup System 8 32 mm. MatrixNEURO Introduction The aim of surgical fracture treatment is to reconstruct the bony anatomy and restore its function. According to the AO, internal fixation is distinguished by anatomical reduction, stable fixation, preservation of blood supply, and early, active mobilization. Plate and screw osteosynthesis has been established and. Tous les catalogues et fiches techniques (PDF) Depuy Synthes. Reclaim Surgical Technique. 44 Pages. DESIGN RATIONALE AND SURGICAL TECHNIQUE. 28 Pages. PRODUCT RATIONALE AND SURGICAL TECHNIQUE. 32 Pages. Speed. 2 Pages. attune. 80 Pages. HAMMERLOCK® 2. 2 Pages. DePuy Glenoid Solutions

Design Rationale. Stiff 64% Tight 54% ainfulP 39% Numb 26% Grinding 21% eakW 21% Unstable 17% Foreign 15%. 0% 20% 40% 60% 80% 100% Adjectives dissatisfied patients use to describe . their knee following TKA. 3. Recreating the Feel of a Healthy Knee. Although Total Knee Arthroplasty has long. Design Rationale GLOBAL DePuy Synthes Joint Reconstruction glenoid products have been designed with a constant 6 mm diametric mismatch between the glenoid and the humeral head component that: • Is designed to emulate anatomic biomechanics of a healthy shoulde Air Pen Drive. Universal pen-shaped power tool system for use in hand, forefoot and maxillofacial surgery. Ergonomic handpiece with powerful motor - Powerful air-cooled motor with up to 60 watts output power and 60'000 rpm at 6.5 bar for efficient and precise osteotomies - Robust, durable and ergonomic stainless steel casing - Universal and machine-washable handpiece Hand Switch Rotary.

ANTHEM Total Knee System Design Rationale 2 • The ANTHEM knee system is a total knee prosthesis with advanced femoral and tibial anatomic design to promote improved anatomic implant fit, taking into consideration the anatomical differences among global ethnicities1 • The ANTHEM knee is based upon trusted design pedigree incorporatin New Jersey LCS Implant/Buechel-Pappas 1981 Pappas and Buechel First mobile bearing design DePuy Agility 1984 Alvine Longest design used in U.S., fixed bearing, semi-constrained, sintered bead surface Scandinavian Total Ankle Replacement (STAR™) 1981/1984 Koefed Fixed bearing, unconstrained, changed to mobile bearing 1984 Third Generatio WARSAW, IN, Sept. 9, 2019 - Johnson & Johnson Medical Devices Companies* announced today that DePuy Synthes** is launching the ATTUNE Cementless Knee in a rotating platform option in select markets around the world.This launch combines the proprietary technologies of the ATTUNE Knee designed to provide stability while the knee is in motion with DePuy Synthes' extensive heritage in rotating.

Guess it makes sense that DePuy is now Pushing a Hip

The Mobility total ankle replacement (DePuy, Leeds, United Kingdom) is an uncemented, 3-component, mobile-bearing design. This article highlights the design rationale and explains the surgical technique with the Mobility implant, as well as offering technical tips and pitfalls gained through personal experiences and literature review 8 9 1 2 5 3 6 4 Delta XTEND™ Design Rationale The Delta XTEND™ System is a total, semi-constrained shoulder arthroplasty that reverses the normal relationship between the scapular and humeral components, moving the scapulo-humeral joint center of rotation medially and inferiorly, increasing the deltoid lever arm a Model names: DePuy ReClaim® Reamer Extension In March 2013, DePuy Orthopaedics, Inc. issued a voluntary device correction for the RECLAIM® Distal Reamer Extension (2975-00-500) due to the potential for one or both of the tabs on the original design to break off and potentially be left in the patient. The RECLAIM® Distal Reamer Extension has bee

Design Rationales Golden State Orthopaedic

  1. The substantial equivalence of the subject RECLAIM Revision Hip System is demonstrated by similarities in intended use, indications for use, materials, geometry, design and performance as compared to the predicate devices. The changes presented in this 510(k) do not present new issues of safety or effectiveness
  2. 3.1. Introduction. This chapter summarizes the design rationale for the DePuy (Leeds, UK) ASR TM (Articular Surface Replacement) system (Isaac et al., 2006), even though this design (October 2009) has been subject to a general recall together with the total hip ASR XL system.Despite the recall, this chapter was included with the other hip resurfacing chapters because the lessons learnt.
  3. The PS design incorporates a polyethylene intercondylar post which compensates for the resected posterior cruciate ligament. This post engages the corresponding femoral component receptacle enabling roll back. The PFC design was first released in 1996, nearly 1/3 of a million have been implanted. It has a 3.58% cumulative percentage probability.
  4. From February 2003 to May 2013, for instance, the top six knee implant manufacturers issued 709 recalls due to flaws in the design or construction of their devices, and a whopping 277 (38%) of these recalled devices belonged to DePuy, the second-largest manufacturer of artificial knee and hip implants in the world
  5. baseplate was introduced. Although a design much ahead of its time, axial compression tests would later show failure of the prosthesis.2 Later in the 1970s the first mobile-bearing knee was created. Its designers, Drs. Buechel and Pappas, aimed to design a mobile-bearing, metal-backed knee system with lo
  6. Design Rationale} 3 {Surgical Technique} STEP 1 Positioning the Patient Place the patient in beach chair position on the operating table. Facilitate clavicle and shoulder access using a radiolucent shoulder-positioning device (Figure 1). An image intensification device or C-arm guides pi

® Total Ankle System - Design Rationale Modern ankle replacement implants consist of two or three components, fixed or mobile-bearing designs with metallic tibial and talar components, stabilized with or without cement. They improved the accuracy of placement, immediate stable fixation to bone, and were a better anatomic match Triathlon ® Design Rationale Motion Hyperextension/Extension Active Flexion Stryker's single radius knee is designed to replace the way the knee moves.1-3 Traditional theory used a direct lateral view of knee motion to characterize the shape of the posterior condyles

The assessment involves the preparation of a design dossier by or on behalf of the manufacturer, which is then submitted to the BSI for review. To give some idea of the scope of such dossiers, the C-Stem Design Dossier included the following standard sections, (1) Executive Summary, (2) Declarations of Conformity, (3 Compatible with complete DePuy glenoid range. The Global AP™ press fit stem system is the outcome of 15 years clinical experience with the Global® shoulder prosthesis. Its fully anatomic design and intuitive surgical technique assist the surgeon to achieve appropriate joint biomechanics, implant stability and range of motion for th 2 DePuy Synthes C-STEM AMT Product Rationale and Surgical Technique The C-STEM AMT Triple Taper Stabilised Hip builds upon the clinical success of the original C-STEM Triple Taper Stabilised Hip and its highly polished design. The functional intra-medullary geometry has been preserved. Th

DePuy hip replacements have a very high rate of failure and side effects due to their metal-on-metal construction. The attorneys at McIntyre Law have spent years representing clients who are victims of faulty hip replacements, and we can help you too. DePuy has already paid out billions to victims of their faulty devices Design History DePuy At the same time, there is tremendous value placed on implant Corail The Alteon HA is a primary hip femoral stem implant, historically categorized by the market as a fully hydroxyapatite (HA)-coated, tri-taper design. This design was based off the DePuy Corail stem of the 1980 Sacral Bars. Fixation of the posterior pelvis in cases of fractures or sacroiliac joint dislocations. − Sacral washers prevent the rounded sacral nuts from pressing into the cortical bone − The sacral bars feature a trocar tip for easy passage through the soft tissues − The sacral bars are fully threaded and are available in 200 mm or 260 mm lengths − The implants are not in direct. • New high mobility humeral cup design. Preserving bone for earlier intervention and faster recovery with: • Curved back metaglene design9. • Fluted modular humeral stem design based on 20 years of DePuy Global® anatomic shoulder history.9 • Modular eccentric epiphysis options for press-fit application Design Rationale have been appointed on the T4 Baggage Reclaim Refurbishment project providing all new glass, stainless steel and micam cladding to the redeveloped baggage hall refurbishment project. March 2011 Design Rationale Awarded Kings Cross Redevelopment Fit Out Contract - COMPLETE

DePuy Synthes RECLAIM Revision Hip System - Quizle

DESIGN RATIONALE AND SURGICAL TECHNIQUE. 28 Pages. Go to the Depuy Synthes website for more information. Other Depuy Synthes products Hip Reconstruction. cemented femoral stem C-STEM™ AMT. primary hip prosthesis CORAIL revision hip prosthesis RECLAIM. The modular design of the RECLAIM Revision Hip System features novel instrument technology that may improve intraoperative handling, flexibility, and efficiency. DePuy's GRIPTION TF Acetabular. Approximately 11,000 ACTIS Hips have been provided for patients globally. The system continues to roll out broadly in 2018. For more information, see the ACTIS Hip System Design Rationale. *DePuy Synthes represents the products and services of DePuy Synthes, Inc. and its affiliates The reduction method will be fracture-specific. Trim plate Trim the plate to the desired length using the bending/ cutting pliers and remove the burrs. Note: If the bending/cutting pliers are used on a plate with preassemble drill sleeves, the drill sleeves must first be removed from the plate. 8 Synthes LCP Compact Hand 1.5 Technique Guide Class 2 Device Recall RECLAIM DISTAL TAPERED. RECLAIM Taper Protector Sleeve. RECLAIM Revision Hip System Orthopedic Manual Surgical Instrument, used to ensure the locking taper surface of the Distal Stem is protected during proximal preparation. Product # 297500110 Lot # 126559; 126569, 181990, 181995, 224156, 231487, 240683, 260366, 260370.

The ACTIS® Total Hip System from DePuy Synthes is Designed to Improve Initial Implant Stability in Total Hip Replacement Unique design features, extended range of stem sizes and improved surgical. Most implant companies makes a stem with this design. Smith & Nephew - Redapt, DePuy - Reclaim, Stryker - Restoration, Biomet - Arcos , Zimmer - ZMR or Wagner SL. Bone Preserving. This design refers to an approach for metaphysial for ingrowth that attempts to preserve bone by performing a high femoral neck cut The Corail femoral stem is a tapered titanium stem with a proximal flared design allowing for a 3-dimensional metaphyseal fit. 11 Stability is achieved through initial press fit and secondarily via fixation through the bone-hydroxyapatite interface. 11, 12 The extensive hydroxyapatite coating increases biological fixation and allows for even. Learn reclaim with free interactive flashcards. Choose from 181 different sets of reclaim flashcards on Quizlet

The rationale for short stems in cementless total hip arthroplasty (THA) is proximal load transfer and absence of distal fixation resulting in preserved femoral bone stock and avoidance of thigh pain. We report a consecutive series of 65 THAs inserted mainly for osteoarthritis with the DePuy Proxima The design of the highly polished, chromium cobalt tibial component and the polyethylene insert in the P.F.C. Sigma RP-F is identical to the P.F.C. Sigma rotating-platform system in terms of the. DePuy Orthopaedics, Inc., a Johnson & Johnson company, is a leading global provider of orthopaedic devices for hip, knee, trauma and extremities, as well as bone cement and operating room products. It is part of the DePuy Family of Companies, which has a rich heritage of pioneering a broad range of products and solutions across the continuum of.

DePuy Synthes, part of the Johnson & Johnson Medical Devices Companies, today introduced the ACTIS Total Hip System in the US at the 2018 American Academy of Orthopedic Surgeons Annual Meeting in. The DePuy Global Advantage® Cuff Tear Arthropathy (CTA) humeral head prosthesis is indicated for use in patients with a massive, irreparable rotator cuff tear and arthritis (Figure 1A). Unlike other humeral heads, this prosthesis has a larger area of lateral articulation. Since most patients with massive rotator cuff tears have proxima Sizing Rationale In the frontal plane, the size increment is smaller for small sizes than between larger sizes allowing fine adjustment in small femoral canals. The Avenir brand includes cementless and cemented stems in standard and lateral versions with a constant CCD angle of 135°. Each range includes 9 sizes, from 129 to 177 mm stem length The LEGION Total Knee System is a comprehensive system designed to allow surgeons to address straightforward primary to complex revision knee arthroplasty. By virtue of its unique implant design features, proprietary materials and intuitive instrumentation, LEGION empowers surgeons to manage diverse surgical challenges and provide personalized joint care with one system, one company Page | 1 Urgent Field Safety Notice (FSN) Product Name: RECLAIM® Taper Sleeve Protector Instrument Type of Action: Field Safety Notice. Date: June 2014 Attention: Orthopaedic Surgeons who use the RECLAIM® Taper Protector Instrument Model names: RECLAIM® Taper Protector Instrument Background: DePuy Orthopaedics, Inc. is issuing a Field Safety Corrective Action and Field Safety Notice on al

DePuy Orthopaedics, Inc. announced in a press release that it has received 510(k) clearance from the FDA for use of the RECLAIM Revision Femoral Hip System in cementless hip revision surgery. Grammont reverse prosthesis: Design, rationale, and biomechanics Pascal Boileau, MD, Duncan J. Watkinson, FRCS, Armodios M. Hatzidakis, MD, and Frederic Balg, MD, FRCSC, Nice, France Combined destruction of the rotator cuff and the gleno-humeral joint may lead to a painful and pseudo-paralyzed shoulder. In this situation a nonconstraine DePuy lost another Pinnacle lawsuit in November 2017 when a federal jury ordered the company to pay $247 million to six patients. The jury found that the implants had a defective design and the company failed to warn consumers about the risks of these devices DePuy Synthes launched the ATTUNE Revision Knee System in the U.S. at the 2018 American Academy of Orthopaedic Surgeons Annual Meeting in New Orleans on March 6.. Here are four things to know. 1. The launch is intended to complement the ATTUNE Primary Knee System and provide surgeons with a comprehensive knee replacement solution Design Rationale Proper fit in the humeral canal aids in proper varus-valgus alignment. Proper fit in the metaphysis, combined with the collar, provides stability against subsidence. The four fins provide additional rotational control. A unique system of humeral cutting and broaching instruments helps achieve optimal alignment and stability wit

Tutti i cataloghi e le schede tecniche Depuy Synthes

NEW ORLEANS, March 7, 2018 /PRNewswire/ -- DePuy Synthes*, part of the Johnson & Johnson Medical Devices Companies**, today introduced the ACTIS® Total Hip System in the US at the 2018 American. This article presents a procedure whereby a second-phase design DePuy Alvine Total Ankle Prosthesis underwent revision to an Agility LP custom-designed stemmed tibial and talar component total ankle replacement system. The rationale for this procedure, the process of developing the custom components, the operative sequence of events, and. A single-surgeon retrospective review of primary PFC Sigma (DePuy Synthes, Warsaw, Indiana) or Attune TKA (DePuy Synthes) was performed. A total of 114 PFC Sigma and 103 Attune implants were analyzed at a mean 3.2 years follow-up for overall PCC, painful PCC, anterior knee pain (regardless of crepitus), and PCC necessitating revision

MatrixNEURO - Depuy Synthes - PDF Catalogs Technical

  1. Statistical Rationale Development for Validation Process of product/package risk assessment • Medical Device—corporate application of ISO 14971:2007 Application of Risk Management to Medical Devices • Formal risk analysis of SBS. Check out Annex H TIR 22 • Most Risk Analyses and Design FMEA's designate Los
  2. USD666713S1 US29/396,478 US201129396478F USD666713S US D666713 S1 USD666713 S1 US D666713S1 US 201129396478 F US201129396478 F US 201129396478F US D666713 S USD666713 S US D666713S Authority US United States Prior art keywords keel punch tibial keel tibial punch ornamental Prior art date 2011-06-30 Legal status (The legal status is an assumption and is not a legal conclusion
  3. Accolade II's Morphometric Wedge is designed to address modern demands with novel technology by evolving conventional tapered wedge femoral stem design with size specific medial curvature to more closely fit a broad range of bone sizes and shapes of today's patient population. 1 Accolade II has been shown to allow for enhance stability, 2 decreased intraoperative femoral fractures, 3 as.
  4. SERF was created in 1973 to facilitate the design and manufacture of orthopedic implants. According to Aaron Villaruz, global platform leader for DePuy Synthes hips, SERF was the company that developed the first dual mobility hip system with the late Professor Gilles Bousquet, M.D., professor at the University Hospital of Saint-Etienne (France.
  5. Introduced to market the Summit® Cemented Stem - the single most successful cemented stem in the history of DePuy by developing the design rationale, surgical technique and sales training manua
  6. stems combine the advantages of straight stem implant design and hip resurfacing. The aim of this chapter is to outline the recent developments in short (metaphyseal) stem arthroplasty. 2. Concise review of the pertinent literature 2.1. Rationale Short metaphyseal femoral stems have been developed in order to improve the results of th
Depuy Synthes/德普 所有产品目录和PDF技术手册

Tous les catalogues et fiches techniques (PDF) Depuy Synthe

GLOBAL UNITE™ Reverse Fracture Implant System Design Rationale DePuy Synthes 3 POROCOAT™ Porous Coating Suture Collar • POROCOAT can be implanted in a press-fit or cemented fashion, enabling intraoperative surgeon choice and flexibility Known today as the DePuy DELTA CTA DELTA XTEND Design Rationale The DELTA XTEND System is a total, semi-constrained shoulder arthroplasty that reverses the normal relationship between the scapular and humeral components, moving the scapulo-humeral joint center of rotation medially and inferiorly

Air Pen Drive - Depuy Synthes - PDF Catalogs Technical

This site complies with the HONcode standard for trustworthy health information: verify here. ShoulderDoc.co.uk satisfies the INTUTE criteria for quality and has been awarded 'editor's choice'. The material on this website is designed to support, not replace, the relationship that exists between ourselves and our patients Design Rationale EXACTECH HIP Surgeon focused. Patient driven.TM. DePuy Tri-Lock BPS 1982 Biomet TaperLoc 1981 DePuy Tri-Lock FIRST GENERATION SECOND GENERATION NEXT GENERATION 2014 EXACTECH ALTEON TAPERED WEDGE EXACTECH ALTEON 2012 Stryker Accolade II. 3 Design History and Evolution of Wedge Stem DePuy recalled the ATTUNE Knee System in 2015. The reason for the recall was the potential for the Balseal, a small wire spring located on the post feature of the ATTUNE Knee Tibial Articulation Surface Instruments used in training, to become damaged and disassociate

DePuy Synthes Expands ATTUNE Knee Platform with Cementless

DePuy to develop the ASR. A new hip prosthesis called the Birmingham Hip Resurfacing (BHR), designed by UK surgeon Derek McMinn, had entered the European market in 1997 (the FDA approved it in 2006), and was proving popular. Smith and Nephew acquired it, and DePuy had to design a better product so that it didn't lose market share The tapered-wedge design of the TRI-LOCK BPS Stem ensures intimateimplant to bone contact proximally, providing both rotational and axial stability, while increasing the opportunity for biological fixation to bone. Reduce the hip and assess what adjustments, if any, are depy to ensure stability through a full range of motion The Delta XTEND design is an improvement of the original Delta CTA design. All the principals of Professor Grammont, which are proven to be clinical effective by many medical centers with a follow-up of more than 15 years, are included. The DELTA XTEND has been designed to improve the range of motion and to reduce the scapular notching by.

All Depuy Synthes catalogs and technical brochuresAlle Kataloge und technischen Broschüren von Depuy Synthes

2143 Examples of Basic Requirements of a Prima Facie Case of Obviousness [R-10.2019] [Editor Note: This MPEP section is applicable to applications subject to the first inventor to file (FITF) provisions of the AIA except that the relevant date is the effective filing date of the claimed invention instead of the time of the invention or time the invention was made, which are only. Subsequently, a number of prostheses were introduced based on a reverse ball-and-socket design (Fenlin, Gerard, Kessel, Kölbel, Liverpool, Neer, and Averyll).3, 7, 16, 19, 24, 29 However, most remained essentially experimental, and the only 2 series published in the English-language literature, apart from the Delta, were on the Kessel prosthesis. . Bayley and Kessel 3 reported a series of 31. Depuy Summit Stem Orthopaedicsone Device Reference. No Difference In Reoperations At 2 Years Between Ceramic On. Femoral Diameter And Stem Type Are Independent Risk Factors. Design Rationale Porocoat Duofix Ha. Depuy Sold Toxic Hip Implants Despite Knowing They Could Be. First Ceramic On Metal Total Hip Replacement System Approved The estimated minimum incidence of liner dissociation from our data was 0.35%. Characterisation of dissociated Pinnacle cases (n = 26) revealed 73% were female with an average age of 59 compared to all retrieved Pinnacle cases (n = 212) where 58% were female with an average age of 66 The modular design of the RECLAIM Revision Hip System features novel instrument technology that may improve intraoperative handling, flexibility and efficiency. The modularity of the system offers surgeons numerous options to treat a patient's unique pathology while simplifying the instrumentation required in surgery Global Unique Device ID: 10603295076933. Version (Model) Number: 1975-24-095. Device Name: RECLAIM REVISION HIP SYSTEM CONICAL PROXIMAL BODY CEMENTLESS TENSILE BAR 24mm x 95mm 95mm LOCKING BOLT. Company Name: DEPUY (IRELAND). Brand Name: RECLAIM