Titan™ Modular Shoulder System
Limit uncertainty with a fully interchangeable & modular shoulder system
The surgeon can independently select distal stems and proximal bodies that best match the patient’s anatomy and bone quality.
Fully interchangeable system
- All primary and fracture bodies can be used with either press-fit or cemented stems.
- There are 26 humeral head sizing options available to provide anatomic fit.
- Multiple glenoid options for patients needing total shoulder replacement.
Total Shoulder Arthroplasty or Hemiarthroplasty is indicated for:
- Severely painful and/or disabled joint resulting from osteoarthritis, traumatic arthritis or rheumatoid arthritis.
- Fracture-dislocations of the proximal humerus where the articular surface is severely comminuted, separated from its blood supply or where the surgeon’s experience indicates that alternative methods of treatment are unsatisfactory.
- Other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable (e.g. – revision of a failed primary component).
Shoulder Hemiarthroplasty is also indicated for:
- Ununited humeral head fractures.
- Avascular necrosis of the humeral head.
- Rotator cuff arthropathy.
- Deformity and/or limited motion.
- Muscular, neurologic, or vascular deficiencies that compromise the affected extremity.
- Known metal allergies.
The humeral component is intended for cemented or un-cemented use.
The glenoid component is intended for cemented use only.
The following conditions are contraindications for total shoulder arthroplasty and hemiarthroplasty:
- Active local or systemic infection.
- Inadequate bone stock in the proximal humerus or glenoid fossa for supporting the components.
- Poor bone quality, such as osteoporosis, where there could be considerable migration of the prosthesis and/or a chance of fracture of the humerus or glenoid.
The following condition is a contraindication for total shoulder arthroplasty:
- Absent, irreparable or nonfunctional rotator cuff or other essential muscles.
Regulatory and Legal Information
Products mentioned in this page are CE class III devices.
Ascension Orthopedics, inc.
8700 Cameron road , Suite 100 Austin,
Texas 78754 • USA
Phone: 512-836-5001 / Fax: 512-836-6933
Ascension Orthopedics Ltd.
Biopark, Broadwater Road Walwyn Garden City Herts,
AL7 3AX • United Kingdom
Phone: +44 1763 222505 / Fax: +44 1763 22204
Sales & Marketing EMEA
Integra LifeSciences Services (France) SAS
Immeuble Séquoia 2 97 allée Alexandre Borodine
Parc technologique de la Porte des Alpes
69800 Saint Priest • FRANCE
Phone: +33 (0)4 37 47 59 00
Fax: +33 (0)4 37 47 59 99
firstname.lastname@example.org • integralife.eu
Please contact Integra customer service should you need any additional information on devices classification.
Please read carefully the instructions for use.
All the medical devices mentioned on this document are CE marked according to European council directive 93/42/EEC on medical devices and its relatives, unless specifically identified as “NOT CE MARKED”. Integra and the Integra logo are registered trademarks of Integra LifeSciences Corporation in the United States and/or other countries. Titan is a trademark of Integra LifeSciences Corporation or its subsidiaries.
Availability of these products might vary from a given country or region to another, as a result of specific local regulatory approval or clearance requirements for sale in such country or region.
Last revision date: 19 May 2015. 0326758-1-EN
For complete product information, please see the Instructions for Use accompanying each product.