CoLink® XP Lapidus & Y
Lapidus Plates are indication specific and designed for use in fusions of the first TMT.
- Transverse Compression Screw eliminates need for independent cross-joint screw
- 3 sizes available; Standard, +1mm and +2mm steps
The CoLink® Y Plate is designed to address a variety of midfoot indications and includes our Transverse Compression Screw feature.
Dynamic Transverse Compression
Use of the Transverse Cross-Joint Screw provides mechanical compression across the fusion site to stimulate the fusion process.
UNIQUE, SEE-THROUGH PLATING
CoLink® View Lapidus
CoLink® View Compression Inserts
The CoLink® View transparent PEEK hub provides efficient cross-joint compression via a 3.5mm Transverse Lag Screw. The low-profile anatomic design provides mechanical compression across the fusion site to stimulate bone fusion. An alternate Titanium Compression Slot design offers a traditional compression ramp to achieve mechanical compression.
CoLag® CS Screws
3.0, 4.0 and 5.0mm Diameter
The CoLag® Screw design unites the rotational stability of a headless screw with the compression lag of a headed screw. The differential threads combined with a low profile head apply a compression lock to the fragment.
Most Significant Screw Innovation in 25 Years
I.B.S. Compression Screws
3.0, 3.5 and 4.5mm
INDIVIDUALLY PACKAGED – Compression Screws are delivered in STERILE, cylindrical cases enclosing a series of capped sleeves. Each Screw package includes a series of self-adhesive labels for UDI compliance and comprehensive implant TRACEABILITY for hospital and patient records.
Each sterile screw package has 6 self-adhesive labels per Implant and is easily identifiable by style, diameter and length on the color-coded end cap.
Each blister pack contains all the necessary instruments for implanting: 2.0, 2.5, 3.0 and 3.5mm Compression Screws.
SUPERELASTIC COMPRESSION STAPLE
CoLink® Bone Graft Harvester
Delivered in sterile, single-use kit for rapid harvest
Morselizes bone into chips to facilitate void filling
Available for use with Tribio® Backfill Plug
to fill corresponding voids
UNIQUE BONE VOID FILLER
Tribio® Backfill Plugs
Delivered sterile and ready-to-use
Osteoconductive scaffold rapidly absorbs the surrounding blood and fluids to aid in new bone formation
Tribio® Backfill Plugs are a proprietary material delivered sterile and ready for use in any bony voids or gaps of the skeletal system. Consisting of hydroxyapatite, tri-calcium phosphate and bioactive glass in a collagen matrix, the Backfill Plugs are sized to easily fit in surgically created osseous defects; 5.5mm dia. (for 6mm void) and 7.5mm dia. (for 8mm void) by 40mm in length. The osteoconductive scaffold rapidly absorbs the surrounding blood and fluids to aid in new bone formation during the healing process.
Demineralized Moldable Bone Putty
AlloAid Crunch, DBM Putty
- Available in flowable, formable putty and crunch in syringe
- Donor recovery and screening performed according to AATB and FDA guidelines
- Crunch consists of DBM putty & cortical cancellous bone chips
100% Cancellous Bone Sponge Cubes
- Moldable, sterile, demineralized/compressive bone matrix
- Cut and molded as needed, sponge-like fit and fill capabilities
- Natural porous scaffold encourages osteoconductivity and promotes vascularization and stimulates new bone growth
- Add bone marrow aspirate or platelet rich plasma to create a composite graft
Representation of SAL (Sterility Assurance Level). Designates the occurrence of a living microorganism surviving the sterilization process. SAL of 10-6 designates the possibility of finding an unsterile product will be 1 in a million. While other sterilization methods have also been shown to inactivate viruses, they can be detrimental to the biological and physical properties of allograft bone.
Bioactive Glass with DBM Putty
A Synergistic Combination of Bioactive Glass & Demineralized Bone Matrix
BioV® Bioactive Matrix is a novel bone graft substitute expressly designed to optimize surgical handling, graft stability and osteoproductivity.
KNOW YOUR PRODUCT SAL. The AlloAid® DBM is terminally sterilized using a validated gamma irradiation process at an SAL (Sterility Assurance Level) of 10-6. This representation of SAL illustrates the occurrence of a living microorganism surviving the sterilization process. SAL 10-6 designates the probability of finding an unsterile product to be 1 in a million. Competitive tissue products may be sterilized to an SAL of 10-3. This increases the odds of finding an unsterile product to 1 in 1000.