Abyrx Montage
An FDA-cleared, settable (hardening) bioabsorbable polymer and hydroxyapatite/ beta tricalcium phosphate-based putty, for use in the control of bleeding from bone during spine, orthopedic, trauma, craniomaxillofacial, thoracic, and other surgical procedures.
MONTAGE is packaged as two individual putties that, upon being hand-mixed for a minimum of 45 seconds, form a cohesive putty (hand moldable and shapeable) of uniform light tan color and consistency for immediate application to bleeding bone.
A fully-mixed MONTAGE putty can be partitioned into pieces for use in different locations. Any subsequent recombination of the divided putty should be completed shortly after mixing, as MONTAGE begins to harden in minutes following mixing.
Once applied, the cohesive MONTAGE putty interdigitates, adheres, and expands into the pores of the bone to control bleeding and remain in place as it begins to set (harden), even under normal irrigation conditions.
Following implantation, MONTAGE will absorb tissue fluid from the surgical site into the micro and macro-porosity of the hardened putty.
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Also related to Craniotomy procedure:
In addition to treating Craniotomy, the Abyrx Montage can also be used in the following procedures:
Chondral Defect (Ankle), Cranial Reconstruction (Cranial Reconstruction), Cranioplasty (Craniotomy/Cranioplasty)