ALLOMATRIX® Injectable DBM Biocomposite

ALLOMATRIX
®
Injectable DBM Biocomposite
ALLOMATRIX®
Injectable DBM Biocomposite
PROPRIETARY
process
ALLOMATRIX® INJECTABLE DBM BIOCOMPOSITE:
A HIGH DBM DOSAGE THAT STAYS IN PLACE
OSTEOSET®
Surgical Grade
Calcium Sulfate
ALLOMATRIX® Injectable DBM Biocomposite is a combination of
demineralized bone matrix (86% by volume) with the properties
of OSTEOSET® surgical-grade calcium sulfate. This combination
provides optimal characteristics for guided bone regeneration.
The combination of these materials enables rapid and reliable
bone repair.
ALLOMATRIX® DBM Biocomposite is a DBM-containing putty
that is provided in a powdered form (i.e. not pre-hydrated).
This preserves the bone morphogenetic protein (BMP) activity
BIOASSAYED
Demineralized
Bone Matrix
until the point of use.1
ALLOMATRIX® DBM Biocomposite is a potent DBM biocomposite
providing desired handling characteristics and fluid resilience.
The dry powdered form of ALLOMATRIX®
Biocomposite preserves BMP activity and
facilitates its unique 5-year
shelf life.
1
Carpenter JF, et. al. Rationale Design of Stable
Lyophilized Protein Formulations: Some Practical
Advice. Pharm Res 1997; 14(8): 969-975.
. . . A RELIABLE DBM BIOCOMPOSITE
osteoinduction / bioassay
contourability
To ensure osteoinductivity of the final
product, each lot of DBM is bioassayed
in vitro utilizing a BMP-2 assay with
criteria that have been correlated
to bone formation in ectopic sites
in a rat model.*
The handling properties
of ALLOMATRIX® Putty
provide contouring
ability for guided bone
regeneration.
injectability
robustness
With the provided syringe, ALLOMATRIX®
Putty can be easily injected into the
bone defect.
To maintain contour and
position, the formulation for
ALLOMATRIX® Putty has been
designed to provide resiliency
in the presence of body fluids
and irrigation solution.
*Data on file.
ALLOMATRIX®
Injectable DBM Biocomposite
ORDERING INFORMATION
ALLOMATRIX®
INJECTABLE PUTTY
Uses
•Open bone voids/gaps not intrinsic
to stability of bony structure
•Extremities and pelvis
8600-0100
1CC
1 EA
8600-0500
5CC
1 EA
•Surgically created osseous defects
8600-1000
10CC
1 EA
•Traumatic injury bony defects
8600-2000
20CC
1 EA
•Augment provisional hardware
Please refer to package inserts for complete indications,
contraindications, precautions and warnings.
Wright Medical Technology, Inc.
1023 Cherry Road
Memphis, TN 38117
800 238 7117
901 867 9971
www.wmt.com
Wright Medical EMEA
Atlas Arena, Australia Building
Hoogoorddreef 7
1101 BA Amsterdam
the Netherlands
011 31 20 565 9060
™Trademarks and ®Registered marks of Wright Medical Technology, Inc.
©2013 Wright Medical Technology, Inc. All Rights Reserved.
008909A 09-Nov-2013