Shoulder Arthroplasty
The most common indications for Shoulder Arthroplasty, Shoulder Joint Arthroplasty and Shoulder Joint Replacement Arthroplasty are: Non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis, Rheumatoid arthritis, Revision where other devices or treatments have failed, Correction of functional deformity, Fractures of the proximal humerus, where other methods of treatment are deemed inadequate; Difficult clinical management problems, including cuff arthropathy, where other methods of treatment may not be suitable or may be inadequate.
BIOTEK offers URSA-Hemi Shoulder Arthroplasty System, Shoulder Joint Arthroplasty and Shoulder Joint Replacement Arthroplasty designed for hemiarthroplasty of the shoulder.
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URSA - Hemi Shoulder Arthroplasty System Item Code: Shoulder-Arthroplasty-System Approximately 60% of all shoulder joint arthroplasty and shoulder joint replacements arthroplasty result from proximal humeral fractures. A proximal humeral fracture is a break to the ball at the top of the upper-arm bone. These fractures typically occur when people fall on an outstretched hand. The URSA Hemi-Shoulder Arthroplasty System, Shoulder Joint Arthroplasty and Shoulder Joint Replacement Arthroplasty was developed and designed to enable surgeons to repair broken bone while replacing the damaged shoulder joint. The URSA Hemi-Shoulder Arthroplasty System can allow patients to regain shoulder movement while reducing or eliminating pain. The URSA Hemi-Shoulder Arthroplasty System designed for hemiarthroplasty of the shoulder has enjoyed nearly a decade of clinical success. The variety of head types and sizes, allow the surgeon to better recreate the normal anatomy which is so important in tensioning of the soft tissues for joint stability and providing maximum postoperative function. The modular components also allow the surgeon to better reconstruct the rotator cuff tuberosity mechanism in difficult acute fractures and chronic malunions of the proximal humerus. The modular design enables the surgeon to easily revise a hemiarthroplasty by allowing unobstructed access to the glenoid. The modularity in both the implants and instruments, along with the numerous design options throughout, increase intraoperative flexibility, offering the surgeon an excellent overall system to perform arthroplasty tailored to each patient.
Size options | URSA HEMI-SHOULDER ARTHROPLASTY SYSTEM,IMPLANT RANGE | | BUS-28.65 | URSA™ humeral stem,small,6.5mm,SS | | BUS-28.75 | URSA™ humeral stem,medium,7.5mm,SS | | BUS-28.85 | URSA™ humeral stem,large,8.5mm,SS | | BUS-29.40.15 | URSA™ humeral head,dia.40mm,neck length 15mm,SS | | BUS-29.40.20 | URSA™ humeral head,dia.40mm,neck length 20mm,SS | | BUS-29.40.22 | URSA™ humeral head,dia.40mm,neck length 22mm,SS | | BUS-30.44.15 | URSA™ humeral head,dia.44mm,neck length 15mm,SS | | BUS-30.44.17 | URSA™ humeral head,dia.44mm,neck length 17mm,SS | | BUS-30.44.20 | URSA™ humeral head,dia.44mm,neck length 20mm,SS | |  | Ask for Quote | |
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