Arcos Modular Femoral Revision System - Biomet Archos Glamour... · The Arcos Modular Femoral...
Transcript of Arcos Modular Femoral Revision System - Biomet Archos Glamour... · The Arcos Modular Femoral...
Arcos Modular Femoral Revision System
Arcos System
The Arcos Modular Femoral Revision
System meets the demands of complex
hip revision surgery by offering
surgeons and OR staff the ability to
customise both the hip implant and
its corresponding instruments in a way
that addresses patient and practice
needs.
The Arcos System’s three proximal
and five distal geometry options
provide surgeons 117 proximal/distal
combinations and multiple auxiliary
fixation options for various femoral
defects.
Simplify the Complex
Cone Proximal BodyOffset OptionStandard and high offset options reproduce various patient anatomies without lengthening the leg
Clinically Proven PPS Coating1-4
Allows for initial scratch-fit stability and bone fixation
BoneMaster CoatingDemonstrated significantly greater bone density in Gruen zone 1 compared to identical standard HA coated implants13
Trochanteric Reattachment Bolt HoleAllows for reattachment of the trochanteric fragment directly to the implant, increasing stability and aiding in bony repair
Version ControlProximal body design allows for intraoperative version adjustment independent of distal stem position
Conical DesignAllows for multiple surgical techniques and vertical offset options
STS (Splined Tapered Stem) Distal StemRoller HardeningRoller-hardened tapers provide up to three times more strength in cantilever beam testing than non-roller hardened tapers5
BoneMaster Coating Demonstrated significantly greater bone density in Gruen zone 1 compared to identical standard HA coated implants13
Splined Tapered 3 degree splined tapered design transfers load distally and provides rotational stability6
Grit BlastProvides for potential long-term stability through bone fixation
Stem Design and Length OptionsStraight stem available in 150 and 190mm lengths
Slotted Distal StemRoller HardeningRoller-hardened tapers provide up to three times more strength in cantilever beam testing than non-roller hardened tapers5
BoneMaster Coating Demonstrated significantly greater bone density in Gruen zone 1 compared to identical standard HA coated implants13
PPS Coating1-4
Allows for initial scratch-fit stability and bone fixation
Anatomic BowMatches the natural anatomy of the femur
Coronal SlotDesigned to reduce the risk of anterior impingement, allow for extended distal fixation and reduce thigh pain
Stem Design and Length OptionsBowed stem available in 150, 200 and 250mm lengths
Calcar Proximal BodyOffset OptionStandard and high offset options reproduce various patient anatomies without lengthening the leg
Clinically Proven PPS Coating1–4
Allows for initial scratch-fit stability and bone fixation
BoneMaster CoatingDemonstrated significantly greater bone density in Gruen zone 1 compared to identical standard HA coated implants13
Trochanteric Reattachment Bolt HoleAllows for reattachment of the trochanteric fragment directly to the implant increasing stability and aiding in bony repair
Version ControlProximal body design allows for intraoperative version adjustment independent of distal stem position
Calcar ShelfThree resection options, for differing levels of bone loss, are designed to transfer load from proximal body to medial bone
3
3
Bullet-tip Distal StemRoller Hardening Roller-hardened tapers provide up to three times more strength in cantilever beam testing than non-roller hardened tapers5
BoneMaster Coating Demonstrated significantly greater bone density in Gruen zone 1 compared to identical standard HA coated implants13
PPS Coating1-4
Allows for initial scratch-fit stability and bone fixation
Anatomic BowMatches the natural anatomy of the femur
Polished Bullet-shaped Distal TipA gradual separation from cortex provides for reduction in distal stresses
Stem Design and Length OptionsStraight stem available in 115mm length; bowed stem available in 150, 200 and 250mm lengths
ILS (Interlocking) Distal StemRoller Hardening Roller-hardened tapers provide up to three times more strength in cantilever beam testing than non-roller hardened tapers5
BoneMaster Coating Demonstrated significantly greater bone density in Gruen zone 1 compared to identical standard HA coated implants13
PPS Coating1-4
Allows for initial scratch-fit stability and bone fixation
Anatomic BowMatches the natural anatomy of the femur
Polished Bullet-shaped Distal TipA gradual separation from cortex provides for reduction in distal stresses
Distal Locking Screw HolesProvide for initial rotational stability in complex femoral reconstruction
Stem Design and Length OptionsBowed stem available in 200, 250 and 300mm lengths
Cone
STS
Calcar
Slotted
Bullet-tip
Interlo
cking
1
Broached Proximal BodyOffset OptionStandard and high offset options reproduce various patient anatomies without lengthening the leg
Clinically Proven PPS Coating1–4
Allows for initial scratch-fit stability and bone fixation
BoneMaster CoatingDemonstrated significantly greater bone density in Gruen zone 1 compared to identical standard HA coated implants13
Trochanteric Reattachment Bolt HoleAllows for reattachment of the trochanteric fragment directly to the implant, increasing stability and aiding in bony repair
Version ControlProximal body design allows for intraoperative version adjustment independent of distal stem position
Fit and Fill DesignProvides initial stability and bone contact when deficiencies are minimal
Broach
edETO
The bolt and claw auxiliary implants
allow the surgeon to reattach the
trochanteric fragment in cases
where a trochanteric osteotomy
is necessary. This unique design
allows for the trochanteric fragment
to attach directly to the implant.
Bolt and Claw Auxiliary Option
ETO (Extended Trochanteric Osteotomy) Distal StemRoller HardeningRoller-hardened tapers provide up to three times more strength in cantilever beam testing than non-roller hardened tapers5
Splined Tapered3 degree splined tapered design transfers load distally and provides rotational stability6
PPS Coating1-4
Allows for initial scratch-fit stability and bone fixation
Grit Blast Provides for potential long-term stability through bone attachment
Anatomic BowMatches the natural anatomy of the femur
Dual Mode FixationProvides biologic fixation for the trochanteric fragment and rotational stability for the intact portion of the femur when an ETO is necessary
Stem Design and Length OptionKinked stem available in 250mm length
Arcos Instrumentation
Instrumentation should not limit surgeons’
implant selection or preferred surgical
technique. The 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 the needs of the patient.
Surgeon Preference
Modular Reamer
Trial
Implant
Arcos 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.
Enhanced Intraoperative Efficiency
Biomet Competitor A Competitor B0
5
10
15
20
25
Num
ber
of
Inst
rum
ent
Cas
es
Modular Reamer
The proximal and distal reamer can be combined or used independently to prepare the proximal and distal portion of the femur, based on the desired surgical technique.
Common Implant and Instrument Geometry
Total Number of System Cases
Arcos System – Addressing Complex Situations
In specific cases revision hip surgery involves
both the femur and acetabulum. Biomet
offers implants designed for advanced
fixation, low wear and dislocation resistance
allowing surgeons to address the most
complex revision situations.
Fulfilling Patient Needs
Freedom Constrained Liner
Offers high level of constraint while maintaining optimal range of motion5,7,8
Maximum Range of Motion:114 Degrees
Average Lever-out Force:198 in. lbs.
Arcos System – Addressing Complex Situations
Trabecular Metal is a registered trademark of Zimmer Inc
Regenerex Porous Titanium Construct unites
the proven clinical history of titanium12 with
an enhanced interconnecting pore structure,
resulting in a revolutionary material that provides
for high levels of biologic fixation.5,10
Regenerex material provides for:• Averageporosityof67
percent5
• Optimalporesizerangefrom 100 to 600 microns (average of 300 microns)5
• Highstrengthandflexibility5
• Fixationinasearlyastwoweeks in animal studies5,10
Bone Integration in Similar Animal StudyTwo weeks after insertion, Regenerex implants displayed bony integration and vascularization
52 Weeks26 Weeks16 Weeks4 Weeks2 Weeks
Regenerex Material10
0
20
40
60
80
100
% B
one
In V
oid
Are
a
Bone Integration5,10
Trabecular Metal™11
No testing data available
Regenerex Porous Titanium Construct Provides for Rapid Fixation in Complex Situations
Regenerex Acetabular Augments
Designed to help maximize stability of components in complex reconstruction
Regenerex RingLoc+ Acetabular Shells
Provide high levels of biologic fixation combined with unparalleled locking technology8–10
Any time the liner is removed, it is recommended that the locking ring be removed and replaced with a new one. If the liner is damaged in any way, a new liner should be utilised.
Authorized Representative: Biomet U.K., Ltd. Waterton Industrial Estate Bridgend, South Wales CF31 3XA, U.K.
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This publication and all content, artwork, photographs, names, logos and marks contained in it are protected by copyright, trademarks and other intellectual property rights owned by or licensed to Biomet or its affiliates. This brochure must not be used, copied or reproduced in whole or in part for any purposes other than marketing by Biomet or its authorised representatives. The use for any other purposes is prohibited.
Biomet does not practice medicine and is not responsible nor does it recommend for the selection of any particular orthopaedic implant or surgical technique for use on a specific patient. The surgeon who performs any implant procedure is responsible for determining and utilising the appropriate techniques for implanting prosthesis in each individual patient. © Biomet 2011
Arcos, PPS, STS, BoneMaster and Regenerex are registered trademarks from Biomet Inc.
References 1. McLaughlin, J. et al. Total Hip Arthroplasty with an Uncemented
Tapered Femoral Component. Journal of Bone and Joint Surgery. 6(90): 1290–6, 2008.
2. Rothman, R. et al. Cementless Femoral Fixation in the Rheumatoid Patient Undergoing Total Hip Arthroplasty: Minimum 5 Year Results. Journal of Arthroplasty. 16(4): 415–21, 2001.
3. Keisu, K.S. et al. Primary Cementless Total Hip Arthroplasty in Octogenarians: Two to Eleven-Year Follow Up. Journal of Bone and Joint Surgery. 83: 359, 2001.
4. Rothman, R. et al. Immediate Weight bearing after Uncemented Total Hip Arthroplasty. Clinical Orthopedics and Related Research. 349: 156–62, 1998.
5. Data on file at Biomet. Bench test results not necessarily indicative of clinical performance.
6. Wagner, H. et al. Cone prosthesis for the Hip Joint. Archives of Orthopaedic and Trauma Surgery. 120: 88–95, 2000.
7. Tradonsky, S. et al. Performance Characteristics of Two-piece Acetabular Cups Series II. Scientific Exhibit. 62nd Annual AAOS Meeting. 1996.
8. Mukesh, K. et al. Porous Ti6Al4V Foam Increases Bone Attachment Strength Over a Surface-rounded Ti6Al4V Treatment. Manuscript in preparation for submission for publication. Data on file at Biomet.
9. Fehring, T. et al. Biomet Study. Motion at the Modular Acetabular Shell and Liner Interface. Clinical Orthopaedics and Related Research. 367: 306–14, 1999.
10. Data on file at Biomet. Testing done on animal models.
11. Bobyn, J.D. et al. Characteristics of Bone Ingrowth and Interface Mechanics of a New Porous Tantalum Biomaterial. Journal of Bone and Joint Surgery (British). 81-B(5): 907, 1999.
12. Hahn, H. and Palich, W. Preliminary Evaluation of Porous Metal Surfaced Titanium for Orthopedic Implants. Journal of Biomedical Materials Research. 4(4): 571–7, 1970.
13. Bøe B, Heier T, Snorrason F, Nordsletten L (2006) Change in bone density and implantation AV Taperloc cementless hip prosthetic with two different hydroxyapatite coatings. A prospective randomized trial. Nordic Orthopaedic Federation 53rd Congress, Oslo, Norway
This publication has been created by Biomet European Central Marketing
Waterton Industrial Estate
Bridgend, South Wales
CF31 3XA, United Kingdom
Tel. 01656 655221Fax: 01656 645454
One Surgeon. One Patient.