Incompass incorporates Adaptis Boney Ingrowth Technology and redesigned instrumentation to support long-term fixation, surgical flexibility and streamlined workflow.
TRIGEN MAX offers trauma surgeons the choice of side-specific (right and left) nails for anatomic screw trajectories.
The first patient is treated in the investigational device exemption clinical trial of HYDRAFIL for disc augmentation.
Incompass incorporates Adaptis Boney Ingrowth Technology and redesigned instrumentation to support long-term fixation, surgical flexibility and streamlined workflow.
TRIGEN MAX offers trauma surgeons the choice of side-specific (right and left) nails for anatomic screw trajectories.
The first patient is treated in the investigational device exemption clinical trial of HYDRAFIL for disc augmentation.
PearlMatrix Bone Graft is the first and only bone growth accelerator proven to accelerate lumbar fusion.
Exactech’s Alteon Stem is a next-generation solution designed to fit a broader range of femoral anatomies while conserving distal bone.
These additions to the VOLT portfolio are anatomically designed for two of the most commonly fractured bones.
A U.S. IDE study is comparing the Freedom Knee with a PEEK-OPTIMA femoral component to a controlled registry of the same system using traditional metal femoral components.
The modular, low-profile construct offers spine surgeons a flexible fixation solution for lateral and anterolateral lumbar fusion.
TrueLok Elevate features a patented design for use in the TBT procedure to provide a limb preservation treatment option for bony or soft tissue deformities or defects.
The GMReis Fibula Nail offers a solution for specific applications where a minimally invasive approach is critical.
The application will work in tandem with ChoiceSpine’s navigation-enabled instrumentation, like the Thunderbolt and Lancer pedicle screws.
OSSIOfiber 2.5mm Suture Anchors support a range of several procedures, including Brostrom repair for lateral ankle instability.
The DEXA-C system has been successfully used in more than 1,500 cervical spine procedures across the United States.
Patients implanted with the FlareHawk Interbody Fusion System may be safely scanned under the conditions outlined in the FlareHawk Instructions for Use.
The system offers a broad expansion range in height, width and now lordotic shape for the expandable spinal implant market.
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