Alliance Spine continually enhances and develops the best products to treat spinal disorders and to promote quicker recovery and better healing.
At Alliance Spine, we have one goal; continually enhance and develop the best products available to treat spinal pathologies, including combining regenerative medical technologies with spinal hardware products to promote faster healing and improve patient outcomes.
05/11/2022
OsteoPro™ DBM 100 Quality
Stringent tissue donor screening, recovery, storage and shipping guidelines are followed to best preserve the grafts for their intended functions.
- Sterility Assurance Level (validated to SAL 10-6 in accordance with ISO 11137-2 Method 1)
- Meets the exacting FDA regulations and AATB standards
- Only donors whose screenings serologic, and microbiologic tests meet or exceed FDA and AATB standards are accepted for transplantation
- Proprietary demineralization processes
Head to our website to learn more.
Inspiring Solutions Through Innovation
05/08/2022
Happy Mother's Day from all of us here at Alliance Spine!
05/04/2022
Founded and under the direct leadership of our four executives, Alliance Partners, LLC (dba Alliance Spine) is a private company, that began its operations in 2010, with a commitment to provide orthopedic and neurological medical devices and clinical chemistry and hematology medical equipment.
Keeping pace with the innovations in the medical regenerative space that directly compliment advancement in spinal technologies, Alliance Spine has partnered with leading surgeons, state of the art manufacturers of human tissue and allografts, and our own proprietary innovations to provide single source quality solutions in the area of orthopedics and regenerative therapies.
Quality is the cornerstone of our commitment to achieve our goals to be the turn-key, “go-to” for our surgeons to achieve consistent favorable outcomes for patients.
Visit our website to learn more. alliance-spine.com
04/27/2022
The Nakoma® ACP System is intended for anterior intervertebral screw fixation of the cervical spine at levels C2-T1.
The Nakoma® ACP System is indicated for use in the temporary stabilization of the anterior spine during the development of cervical spinal fusion in patients with the following indications:
Degenerative Disc Disease (as defined by neck pain of discogenic origin with degeneration of the disc confirmed by patient history and radiographic studies)
Trauma (including fractures)
Tumors
Deformities or curvatures (including kyphosis, lordosis, or scoliosis)
The Alliance Spine team wishes you a happy Easter filled with happiness and lots of chocolate!
04/06/2022
Cyclone®
A Bone Marrow Concentrate System that utilizes a proprietary system of gentle centrifugation and protection of the delicate buffycoat layer to produce superior cell yields for Bone Marrow Concentrate (BMC).
The Cyclone Advantage:
- Highly Concentrated Bone Marrow Cells produces a much greater amount of BMC using light centrifugal acceleration and gentle deceleration.
- Sterile System requires only two sterile barrier entries and ensures sterility through a sterile collection tube, processing in the centrifuge, and channeling the marrow through a closed system.
- Versatile and Portable processes from 30 – 240mL of bone marrow aspirate in 15 minutes and is easily transferred from one operating room to another.
03/30/2022
The Cannulated Aspiration Screw consists of a Cannulated Aspiration Screw, Stylet and Luer Lock. The luer lock is intended to allow bone marrow biopsy/aspiration.
The components of this device are composed of surgical grade stainless steel per ASTM F899.
Promote OsteoStrip® is a pliable and absorbable cancellous bone graft that also exhibits osteoconductive and osteoinductive properties.
These characteristics used as a homologous tool for bone grafting in spinal fusions, non-unions, and bone fractures. OsteoStrip® is processed using a next generation proprietary processing method that maintains the interconnected structure of trabecular bone.
Use with Alamo® C, Alamo® T, Alamo® P, and Nakoma®-SL for optimal results.
AmnioStrip® is comprised of placental tissue allowing it to be effective at protecting a wide variety of wounds, while simultaneously creating an environment conducive to the regeneration of healthy tissue.
Versatile tissue with application in a variety of surgical procedures. Literature has documented amnion contains collagen, has a variety of growth factors, is compatible and absorbs within the body.
Use with Alamo® C, Alamo® T, Alamo® P and Nakoma®-SL for optimal results.
To all the incredible women in the world, shine on, not just today but every single day!
Happy International Women's Day from the Alliance Spine team!
03/02/2022
Our Product: Alamo® P
Indications for Use
The Alamo® P is intended for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) at one or two contiguous levels of the lumbosacral spine (L2-S1).
DDD is defined as back pain of discogenic origin with the degeneration of the disc confirmed by history and radiographic studies.
02/23/2022
Alamo C
Anterior cervical intervertebral device manufactured from PEEK Optima® LT1 with tantalum markers for radiographic visualization.
Indications for Use
The Alamo® C is indicated for anterior cervical interbody fusion procedures in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one level from C2-T1.
DDD is defined as discogenic pain with the degeneration of the disc confirmed by history and radiographic studies.
These patients should have had six weeks of non-operative treatment prior to treatment with an intervertebral cage.
The device system must be used with supplemental fixation and autograft to facilitate fusion and is to be implanted via an open, anterior approach.
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At Alliance Spine, we have one goal; continually enhance and develop the best products available to treat spinal pathologies, including combining regenerative medical technologies with spinal hardware products to promote faster healing and improve patient outcomes.
OUR HISTORY, OUR PARTNERS AND COMMITMENT TO QUALITY
Founded and under the direct leadership of our four executives, Alliance Partners, LLC (dba Alliance Spine) is a private company, that began its operations in 2010, with a commitment to provide orthopedic and neurological medical devices and clinical chemistry and hematology medical equipment.
Keeping pace with the innovations in the medical regenerative space that directly complement advancement in spinal technologies, Alliance Spine has partnered with leading surgeons, state of the art manufacturers of human tissue and allografts, and our own proprietary innovations to provide single-source quality solutions in the area of orthopedics and regenerative therapies.
Quality is the cornerstone of our commitment to achieve our goals to be the turn-key, “go-to” for our surgeons to achieve consistently favorable outcomes for patients.
QUALITY STATEMENT AND REGULATORY COMPLIANCE
At Alliance Spine, we are committed to complying with regulations and to meeting customer needs. We are "Inspiring Solutions through Innovation" by striving for continual improvement in our process approach.
We do this by maintaining the effectiveness of the Quality management system, periodically reviewing our objectives and instilling risk management principles throughout the product development lifecycle. We operate within the framework of all applicable regulatory requirements.
Alliance Spine is registered with the FDA and our Quality Management System is ISO 13485 certified. By adopting the ISO 13485 standards, we align our commitment to design a quality management system that establishes and maintains the effectiveness of our processes. It ensures the consistent design, development, production, and delivery of medical devices that are safe for their intended purpose. Our implants interbody systems and regenerative medicine solutions meet or exceed the FDA requirements for manufacturers of safe and effective medical devices. Our Biologics are held to the highest quality and regulatory standards, including but not limited to stringent tissue donor screening, recovery, storage, and shipping guidelines are followed to best preserve the grafts for their intended functions.
Our top tier allografts meet and exceed the exacting FDA Regulation of Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/P's) and American Association of Tissue Banks (AATB) standards.
