Puros-S and - S2 Brochure

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Cervical Solutions

Puros®-S and Puros®-S2


Cervical Interbody Allograft Implants

The solution of choice for cervical interbody implants.


Compatibility
Zimmer Biomet Spine’s Puros cervical allografts give surgeons the power to choose. Sterile-packed
Puros-S and Puros-S2 allow surgeons to select from either one-piece cortical grafts or reinforced cortical
and cancellous combination grafts. The Puros family delivers the shapes, sizes and angles to fit varying
patient anatomies, as well as best-in-class features designed to facilitate insertion, minimize migration
and resist pullout. All Puros products work with versatile instrumentation that simplifies implantation
and improves ease of use.

A PROVEN ALLOGR AF T SOLUTION


Strength
•     Puros-S features the strength of all-cortical bone, while Puros-S2 features
cortical bone with an osteoconductive cancellous center
•     Both Puros-S and Puros-S2 meet stringent quality standards that meet all
U.S. Food and Drug Administration donor screening and testing requirements

Adaptability
•     With three footprints, two geometric options and five heights, Puros-S and
Puros-S2 are designed for varying patient anatomies
•     Between Puros-S and Puros-S2, surgeons can choose between a cortical or
cortical-cancellous implant to best suit patient needs and surgeon preference

Validation
•     Puros constructs are sterilized using RTI Surgical’s proprietary BioCleanse®
Tissue Sterilization Process*
•     Sterilization process has been proven to inactivate or remove pathogens while
preserving the biomechanical integrity of the graft
•     Puros implants must pass stringent donor screening

*BioCleanse is a U.S. registered trademark owned by RTI Surgical, Inc.


EXPERIENCE THE BENEFITS OF PUROS-S AND PUROS-S2

Options to Fit Your Preferences


In addition to both cortical and cortical-cancellous offerings,
all Puros allografts feature a comprehensive assortment of
precisely machined heights and angles to accommodate
your preferences and varying patient anatomies.
Puros-S Puros-S2
Validated Tissue Sterilization Process
Puros constructs are sterilized using RTI’s proprietary
BioCleanse Process. This fully automated, DESCRIPTION LENGTH × WIDTH LORDOSIS HEIGHT

pharmaceutical-grade process has been proven to Puros-S 11 mm × 11 mm 0° | 7° 5 mm | 6 mm | 7 mm


inactivate or remove pathogens such as bacteria, fungi, 11 mm × 14 mm 8 mm | 9 mm | 10 mm
14 mm × 14 mm
viruses and spores while preserving the biomechanical
integrity of the graft. In addition, all Puros allografts are Puros-S2 11 mm × 11 mm 0° | 7° 5 mm | 6 mm | 7 mm
subject to stringent donor screening, and terminal 11 mm × 14 mm 8 mm | 9 mm | 10 mm
14 mm × 14 mm
irradiation that reaches a 10 –6 sterility assurance level.

Compression Test Results Static Compression Testing


Samples were tested to ensure that both Puros-S 16,000
and Puros-S2 assembled constructs could withstand 14,000
Compressive Strength (N)

compressive loads applied in the cervical spine. The 12,000


design goal was to withstand a load equivalent to or 10,000
greater than the ultimate compressive strength of a 8,000
cervical vertebral body (2,000 N).1 Test results of each 6,000
construct far exceeded the compressive strength of 4,000
2,000 N, as shown in the graph at right.2-3 2,000
0
Vertebral Puros-S Puros-S Puros-S2
Body (4-pin)† (2-pin)†

Puros-S constructs reached maximum loads of test machinery without failure.
References:
1. White AA, Panjabi MM. Clinical Biomechanics of the Spine. 2nd ed. Philadelphia: Lippincott,
Williams and Wilkins. 1990.
2. RTI Surgical, Mechanical Testing Report #4912 rev. 0
3. RTI Surgical, Design Verification Summary Report #5531 rev. 0


800.447.3625 zimmerbiomet.com
©2018 Zimmer Biomet Spine, Inc. All rights reserved.
All content herein is protected by copyright, trademarks and other intellectual property rights, as applicable, owned by or licensed to Zimmer
Biomet Spine, Inc. 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 Spine. This material is intended for health care professionals, the Zimmer Biomet Spine sales force and
authorized representatives. 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 www.zimmerbiomet.com.
1068.2-US-en-REV0318

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