Integra. Silicone Toe System SURGICAL TECHNIQUE

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Silicone Toe System SURGICAL TECHNIQUE

Silicone Toe System Table of Contents Indications...2 Contraindications...2 Warnings...2 Precautions...2 Adverse Events...2 Flexible Great Toe (FGT)...3 Surgical Technique...4 Step 1 Sizing and Positioning Guide...4 Step 2 Bone Resection...4 Step 3 Joint Preparation... 5 Step 4 Implant Placement...5 Step 5 Closure... 6 Classic Flexible Great Toe (CGT)...7 Surgical Technique...8 Step 1 Incision and Joint Preparation...8 Step 2 Resection of Phalangeal Base & Soft Tissue...8 Step 3 Soft Tissue and Sesmoid Positioning... 9 Step 4 Implantation... 9 Step 5 Closure...10 The Lesser Metatarsal Phalangeal Implant (LMP)...11 Surgical Technique... 12 Step 1 Incision... 12 Step 2 Joint Preparation... 12 Step 3 Implant Sizing... 13 Step 4 Implant Placement... 13 Step 5 Closure... 14 Ordering Information...Back Cover

Forefoot Implant Arthroplasty Integra offers two options to support reconstruction of the first metatarsal phalangeal joint. The implant for the lesser MP joints provides full anatomic function. Indications The Integra Silicone CGT and FGT devices are indicated for: Hallux limitus or hallux rigidus Painful rheumatoid arthritis Hallux abducto valgus associated with arthritis Unstable or painful joint from previous surgery The Integra Silicone LMP device is indicated for: Partial or complete dislocation of the lesser metatarsophalangeal joint Pain associated with rheumatoid or osteoarthritis Repair of unsuccessful arthroplasties of the lesser metatarsophalangeal joint Stiffness at the lesser metatarsophalangeal joint associated with joint disease Kohler s disease Hammer toe deformity where the proximal phalanx is dorsally located on the metatarsal in a fixed contracture state Contraindications General contraindications for the use of these implants for joint reconstruction include: A psychologically unsuitable patient A patient with skin, bone, circulatory and/or neurological deficiency Nonfunctioning and irreparable musculotendinous system Active sepsis Inadequate bone stock Warnings Strenuous loading, excessive mobility, and articular instability all may lead to accelerated wear and eventual failure by loosening, fracture, or dislocation of the device. Patients should be made aware of the increased potential for device failure if excessive demands are made upon it. Implants are mechanical devices that can be worn away, fatigued or broken. An implant site may become infected, painful, swollen, or inflamed. The status of the adjacent bone and soft tissue may be inadequate to support the implant, or may deteriorate in time resulting in instability, deformity, or both. The benefits from implant surgery may not meet the patient s expectations or may deteriorate with time, necessitating revision surgery to replace the implant or to carry out alternative procedures. Revision surgeries with implants are not uncommon. Precautions This product is provided sterile in an undamaged package and is for ONE TIME USE ONLY. If either the implant or the package appears damaged, expiration date has been exceeded or if the sterility is questioned for any reason, the implant should not be used. DO NOT clean, re-sterilize or reuse as this may damage or compromise performance of the devices and may expose patient to risk of transmitting infectious diseases. Implants should only be handled with blunt instruments to avoid scratching, cutting or nicking the device. Meticulous preparation of the implant site and selection of the proper size implant increase the potential for successful outcome. A complete range of trial sizers is available to aid in bone preparation. It is suggested that the proper size implant be removed from its sterile package only after the implant site has been prepared and properly sized. Adverse Events Potential adverse events reported with toe joint prostheses include pain, loosening, fracture, dislocation, or infection. There have been some reports of patients with silicone sensitivity reactions following joint replacement. Implantation of materials such as silicone may result in foreign body reaction adjacent to the implant site. Injury to the surrounding nerves, blood vessels, tendons, or soft tissues can occur as a consequence of implanting this device. In some patients, wear particles from silicone elastomer implants used in bone and joint reconstruction may participate in, or exacerbate, synovitis or bone cyst complications in contiguous bone. Contributing factors have been reported to include the use of implants in physically overactive patients, associated preoperative pathology such as cysts and degenerative changes, intraoperative temporary stabilization with Kwires, subluxated implants, implant over or undersizing, and uncorrected or recurrent deformity. 2

Flexible Great Toe (FGT) The Flexible Great Toe (FGT) is a third generation flexible implant for first metatarsophalangeal joint arthroplasty. It is constructed of durable UltraSIL silicone elastomer and its anatomically designed hinge allows for free and natural movement of the 1st MP joint. The design incorporates angled osteotomies, allowing for the preservation of the flexor hallucis brevis tendon to function in its natural state. The Flexible Great Toe Advantage Design Feature Advantage Anatomical Hinge The patented axial offset hinge design reduces stress on the prosthesis and improves biomechanical function Angled Osteotomies Flexor hallucis brevis tendon preserving Optional Titanium Grommets Prosthesis Stems Match Canal Shapes Hinge Buttresses Rib on Inferior Aspect of Hinge Allows for intraoperative flexibility to determine the best approach for each patient Phalangeal stem is trapazoidal and metatarsal stem is rectangular A highly engineered hinge offers 95 degree range of motion and prevents the grommets from contacting each other The patented strength rib aids in the overall strength of the construct and gives the implant its signature rigidity 3

As the manufacturer of this device, Integra does not practice medicine and does not recommend this or any other surgical technique for use on a specific patient. The surgeon who performs any implant procedure is responsible for determining and using the appropriate techniques for implanting the device in each patient. Flexible Great Toe Surgical Technique A longitudinal incision is made on the dorsal aspect of the first metatarsophalangeal joint. The incision is deepened by sharp and blunt dissection to the level of the joint, and the vital structures are retracted. A longitudinal capsulotomy is performed, and the joint is dissected free. The base of the proximal phalanx and the head of the metatarsal are completely exposed. All hypertrophic bone is resected from both the metatarsal and phalanx. Any soft tissue contractures must be released as dictated by the deformity. Step 1 Sizing and Positioning Guide 1-1 The cutting guide instrument is then utilized to resect the base of the proximal phalanx and distal portion of the metatarsal head. The tab on the inferior side of the guide is placed within the joint space, and the saw blade is placed in each of the slots of the cutting guide to start the bone cuts. 1-1 Step 2 Bone Resection 2-1 After the appropriate angles have been established, the cutting guide is removed and the bone cuts are completed. 2-1 4

Flexible Great Toe (FGT) Step 3 Joint Preparation 3-1 3-2 A pilot hole is then made in the medullary canal of the metatarsal. The trial sizers are used to chose the correct size implant. The rectangular broach instrument corresponding to the selected trial sizer is utilized to complete the preparation of the medullary canal. A similar procedure is now used to broach the medullary canal of the proximal phalanx, using the appropriate size trapezoidal broach. Range of Motion Test The sizer is now used to check for fit and range of motion. An Accordion Test is recommended to be certain there is no jamming of the implant. This test is performed by loading the foot while holding the hallux in its corrected position and checking the medial side of the joint to see if there is any compression of the sizer in a similar manner as an accordion would be compressed. 3-1 Note If there is compression of the sizer, then inadequate bone has been resected and additional bone is removed from the base of the proximal phalanx. Step 4 Implant Placement 4-1 4-2 When all soft tissue contractures have been released and full range of motion is achieved, the trial sizer is removed and the surgical site is thoroughly irrigated. If the surgeon elects to use grommets, the grommets are press-fit in place using the grommet impactor instrument. The grommets must seat against the resected bone ends without protruding into the soft tissues. 4-1 5

Step 5 Closure 5-1 The appropriate size implant is then inserted. The joint capsule is sutured being certain to completely cover the prosthesis. Wound closure is performed with suture of the surgeon s choice. Bandaging and post-operative management corresponds to other arthroplasty procedures of this joint. 5-1 7 8 9 10 1 2 Picture above is representative of instruments only not actual surgical tray. 6 5 11 4 3 12 20 = Green 30 = Yellow/Orange 40 = Blue 50 = Red Product # 1 FGT-CG2LT 2 FGT-CG2ST 3 FGT-DLT 4 FGT-DST 5 FGT-PLT 6 FGT-PST 7 FGT-205T 8 FGT-305T 9 FGT-405T 10 FGT-505T FGT Cutting Guide - Gen II, Large, Assembly FGT Cutting Guide - Gen II, Small, Assembly FGT System Distal Broach Large FGT System Distal Broach Small FGT System Proximal Broach Large FGT System Proximal Broach Small FGT System Implant Trial Sizer 20 FGT System Implant Trial Sizer 30 FGT System Implant Trial Sizer 40 FGT System Implant Trial Sizer 50 11 FGT-IMPT FGT Impactor 12 MHT-LGTHT Universal Handle FGT-LIDT Lid for FGT Case 17-5075T Base for FGT Case 17-5077T Tray Mat 6.7x1.6 Size (mm) A B C D E F FGT-20T 9.9 13.7 8.9 11.6 12.3 16.3 FGT-30T 9.9 13.7 9.9 12.7 13.5 18.0 FGT-40T 11.9 16.7 10.9 14.0 14.9 19.8 FGT-50T 11.9 16.7 12.0 15.3 16.3 21.6 6

Classic Flexible Great Toe (CGT) The Classic Flexible Great Toe (CGT) is a third generation implant for first metatarsophalangeal joint arthroplasty. It is constructed of durable UltraSIL silicone elastomer and its anatomically designed hinge allows for free and natural movement of the 1st MP joint. The implant requires vertical osteotomies, eliminating the need to use a cutting guide. The Classic Flexible Great Toe Advantage Design Feature Advantage Anatomical Hinge The patented axial offset hinge design reduces stress on the prosthesis and improves biomechanical function Requires Vertical Osteotomies Simple cuts require no cutting guide Anatomically Matched Stems Rib on Inferior Aspect of Hinge Hinge Buttresses The stem geometry is optimized for the unique anatomy of the intramedullary canals of the phalanx and metatarsal bones The patented strength rib aids in the overall strength of the construct and gives the implant its signature rigidity A highly engineered hinge offers 95 degree range of motion and prevents the grommets from contacting each other 7

As the manufacturer of this device, Integra does not practice medicine and does not recommend this or any other surgical technique for use on a specific patient. The surgeon who performs any implant procedure is responsible for determining and using the appropriate techniques for implanting the device in each patient. Classic Great Toe Surgical Technique A longitudinal incision is made on the dorsal aspect of the first metatarsal phalangeal joint. The incision is deepened by sharp and blunt dissection to the level of the joint, and the vital structures are retracted. A longitudinal capsulotomy is performed, and the joint is dissected free. The base of the proximal phalanx and head of the metatarsal are completely exposed. All hypertrophic bone is resected from both the metatarsal and phalanx. Step 1 Incision and Joint Preparation 1-1 An appropriate portion of the distal aspect of the metatarsal head and base of the proximal phalanx are then resected. A pilot hole is made in the medullary canal of the metatarsal. The rectangular broach instrument is used to prepare the medullary canal of the metatarsal. A similar procedure is used to broach the medullary canal of the proximal phalanx, using the trapezoidal broach. The trial sizers are utilized to determine the correct implant size. When all soft tissue contractures have been released and full range of motion is achieved, then the trial sizer is removed. 1-1 Step 2 Resection of Phalangeal Base & Soft Tissue 2-1 The resection of the phalanx base may detach the flexor hallucis brevis tendon. If this occurs, the surgeon should consider performing a flexor tenodesis procedure to maintain functional stability of the joint. A hole is drilled at the inferior aspect of the stump of the proximal phalanx. The flexor hallucis longus tendon is sutured through this hole to the stump of the proximal phalanx. 2-1 8

Classic Flexible Great Toe (CGT) Step 3 Soft Tissue and Sesmoid Positioning 3-1 The flexor hallucis brevis tendon is then sutured to the tendon of the flexor hallucis longus, with the sesmoids in a natural position. 3-1 Step 4 Implantation 4-1 The appropriate size implant is then inserted in the joint. The capsule is sutured being certain to completely cover the prosthesis. 4-1 9

Step 5 Closure 5-1 Surgical site closure is performed with suture of the surgeon s choice. Bandaging 5-1 and post-operative management corresponds to other arthroplasty procedures of this joint. 3 1 4 2 8 5 6 7 Picture above is representative of instruments only not actual surgical tray. 20 = Green 30 = Yellow/Orange 40 = Blue 50 = Red 60 = Gray/White Product # 1 CGT-DST 2 CGT-PST CGT Broach Distal 1-Size CGT Broach Proximal 1-size 3 CGT-205T CGT Sizer Size 20 4 CGT-305T CGT Sizer Size 30 5 CGT-405T CGT Sizer Size 40 6 CGT-505T CGT Sizer Size 50 7 CGT-605T CGT Sizer Size 60 8 MHT-LGTHT Universal Handle 17-5185T Base for CGT Case CGT-LIDT Lid, CGT Case Size (mm) A B C D E F CGT-20T 33.3 15.0 8.8 9.5 12.5 16.0 CGT-30T 36.1 16.2 9.4 10.5 13.5 16.9 CGT-40T 39.6 17.8 10.0 11.8 15.0 17.9 CGT-50T 43.1 20.0 10.7 12.4 15.6 19.0 CGT-60T 47.3 21.5 11.4 13.7 17.1 21.0 10

The Lesser Metatarsal Phalangeal Implant (LMP) The Lesser Metatarsal Phalangeal Implant (LMP) is the first prosthesis designed specifically to supplement lesser metatarsal phalangeal joint arthroplasty. It is constructed of durable UltraSIL silicone elastomer and its anatomically designed hinge allows for free and natural movement of the lesser MP joints. The Lesser Metatarsal Phalangeal Implant (LMP) Design Feature Advantage Anatomical Hinge Minimal Bone Resection The hinge design allows for excellent range of motion without stressing the prosthesis A vertical osteotomy in the metatarsal head is all the cutting that is required Anatomically Matched Stems Rectangular stems match the anatomy of each medullary canal Hinge Buttresses Variable Sizes The hinge design allows for the excellent range of motion without stressing the prosthesis The LMP is offered in four sizes and is supported by an instrumentation set 11

As the manufacturer of this device, Integra does not practice medicine and does not recommend this or any other surgical technique for use on a specific patient. The surgeon who performs any implant procedure is responsible for determining and using the appropriate techniques for implanting the device in each patient. Lesser Metatarsal Phalangeal Surgical Technique Step 1 Incision 1-1 An incision is made on the dorsal aspect of the appropriate lesser metatarsal phalangeal joint. The incision is deepened by sharp and blunt dissection to the level of the joint. A longitudinal capsulotomy is performed and the joint is dissected free. The base of the proximal phalanx and the head of the metatarsal are completely exposed. All soft tissue contractures must be released as dictated by the deformity. 1-1 Note In most cases, the base of the proximal phalanx is preserved. A pilot hole is made through the joint cartilage of the phalanx base. The medullary canal is reamed to accept the distal stem of the implant, using the smaller broach to create a transverse rectangle. Step 2 Joint Preparation 2-1 The distal portion of the metatarsal head is resected at the appropriate level for the existing disease or deformity. A pilot hole is made in the medullary canal and the larger broach is utilized to ream the canal, creating a vertical rectangle to accept the proximal stem of the implant. 2-1 12

The Lesser Metatarsal Phalangeal Implant (LMP) Step 3 Implant Sizing 3-1 The trial sizers are used to select the correct size implant, and to be certain that all soft contractures have been released. It is important to load the foot with the trial sizer in place to be certain there is no jamming of the implant. 3-1 Step 4 Implant Placement 4-1 The sizer is then removed and the wound thoroughly irrigated. The appropriate size implant is then inserted. 4-1 13

Step 5 Closure 5-1 The joint capsule is sutured being certain to completely cover the prosthesis. Wound closure is performed with suture of the surgeon s choice. Bandaging and post-operative management corresponds to other arthroplasty procedures of this joint. 5-1 3 4 5 6 1 2 7 Picture above is representative of instruments only not actual surgical tray. 20 = Green 30 = Orange 40 = Blue 50 = Red Product # 1 LMP-DST 2 LMP-PST 3 LMP- 205T 4 LMP-305T 5 LMP-405T 6 LMP-505T LMP System Distal Broach, One Size LMP System Broach, One Size LMP System Implant Trial Sizer 20 LMP System Implant Trial Sizer 30 LMP System Implant Trial Sizer 40 LMP System Implant Trial Sizer 50 7 MHT-LGTHT Universal Handle LMP-LIDT Lid for LMP Case 17-5189T Base for LMP Case Size (mm) A B C D E F G H I J K LMP-20T 21.1 9.2 6.3 5.6 11.2 2.5 8.0 5.1 2.9 3.6 3.7 LMP-30T 28.3 12.7 8.0 7.6 14.0 3.1 10.0 6.4 3.4 4.4 4.4 LMP-40T 35.1 16.3 9.6 9.2 16.8 3.7 12.0 7.7 3.6 5.2 5.0 LMP-50T 42.0 19.8 11.1 11.1 19.6 4.3 14.0 9.0 4.3 6.1 5.9 14

Silicone Toe System Flexible Great Toe Instruments Reference FGT-CG2LT FGT Cutting Guide - Gen II, Large, Assembly FGT-CG2ST FGT Cutting Guide - Gen II, Small, Assembly FGT-DLT FGT System Distal Broach Large FGT-DST FGT System Distal Broach Small FGT-PLT FGT System Proximal Broach Large FGT-PST FGT System Proximal Broach Small FGT-205T FGT System Implant Trial Sizer 20 FGT-305T FGT System Implant Trial Sizer 30 FGT-405T FGT System Implant Trial Sizer 40 FGT-505T FGT System Implant Trial Sizer 50 FGT-IMPT FGT Impactor MHT-LGTHT Universal Handle FGT-LIDT Lid for FGT Case 17-5075T Base for FGT Case 17-5077T Tray Mat 6.7x1.6 Flexible Great Toe Implants Reference FGTTOTE Flexible Great Toe Tote FGT-20T FGT Implant Size 20 FGT-30T FGT Implant Size 30 FGT-40T FGT Implant Size 40 FGT-50T FGT Implant Size 50 Lesser Metatarsal Phalangeal Implant Instruments Reference LMP-DST LMP System Distal Broach, One Size LMP-PST LMP System Proximal Broach, One Size LMP- 205T LMP System Implant Trial Sizer 20 LMP-305T LMP System Implant Trial Sizer 30 LMP-405T LMP System Implant Trial Sizer 40 LMP-505T LMP System Implant Trial Sizer 50 MHT-LGTHT Universal Handle LMP-LIDT Lid for LMP Case 17-5189T Base for LMP Case Classic Great Toe Instruments Reference CGT-DST CGT Broach Distal 1-Size CGT-PST CGT Broach Proximal 1-size CGT-205T CGT Sizer Size 20 CGT-305T CGT Sizer Size 30 CGT-405T CGT Sizer Size 40 CGT-505T CGT Sizer Size 50 CGT-605T CGT Sizer Size 60 MHT-LGTHT Universal Handle 17-5185T Base for CGT Case CGT-LIDT Lid, CGT Case Classic Great Toe Implants Reference CGTTOTE Classic Great Toe Tote CGT-20T CGT Implant Size 20 CGT-30T CGT Implant Size 30 CGT-40T CGT Implant Size 40 CGT-50T CGT Implant Size 50 CGT-60T CGT Implant Size 60 Lesser Metatarsal Phalangeal Implants Reference LMPTOTE Lesser Metatarsal Phalangeal Tote LMP-20T LMP Implant Size 20 LMP-30T LMP Implant Size 30 LMP-40T LMP Implant Size 40 LMP-50T LMP Implant Size 50 Availability of these products might vary from a given country or region to another, as a result of specific local regulatory approval or clearance requirements for sale in such country or region. n Non contractual document. The manufacturer reserves the right, without prior notice, to modify the products in order to improve their quality. n Warning: Applicable laws restrict these products to sale by or on the order of a physician. n Consult product labels and inserts for any indication, contraindications, hazards, warnings, precautions, and instructions for use. For more information or to place an order, please contact: United States, Canada, Asia, Pacific, Latin America USA 800-654-2873 888-980-7742 fax n International +1 609-936-5400 +1 609-750-4259 fax n integralife.com/contact Manufacturer: Ascension Orthopedics, Inc. 11101 Metric Blvd Austin, TX 78758 n USA Integra and the Integra logo are registered trademarks of Integra LifeSciences Corporation or its subsidiaries in the United States and/or other countries. 2017 Integra LifeSciences Corporation. All rights reserved. Printed in USA. 0M LC-04-1300-0003 Rev. C 0421784-4-EN