Profile: Samo SpA specializes in the development, manufacture and marketing of orthopedic products. We manufacture bone fixation products and joint reconstruction implants. MultiFIT modular system consists of two parts:stem and neck, that can be combined with all reciprocal components in order to enable a precise selection of the size according to the patient's anatomy. The stem presents a cone-shaped cavity just above the osteotomy plane for fixation with the neck component, which in its turn is provided with a morse taper 12/14 for coupling with the femoral head. The total hip replacement system Duofit® consists of five stems and four acetabular cups in titanium, for cementless fixation - offering the physician possible long term results and of three stems in cobalt chromium molybdenum alloy & high nitrogen stainless steel for cemented implants. It meets the specific requirements of the surgeon and of the patient. The possible geometrical variations of the cementless stem, its coating together with the use of different biomaterials, driven to the design of eight femoral implants, meeting all the physician's requirements for each individual medical case. The Trekking total prosthetic knee system is an integrated system, providing the surgeon with a wide range of options to choose the appropriate solution from, for each patient and pathology, thus meeting the requirements of each single clinical case. The Trekking system features biomechanic implants, and avails itself of the different fixation opportunities.
The company was founded in 1939.
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• Non-Electric Biopsy Forceps (FDA Code: FCL / 876.1075) A gastroenterology-urology biopsy instrument is a device used to remove, by cutting or aspiration, a specimen of tissue for microscopic examination. This generic type of device includes the biopsy punch, gastrointestinal mechanical biopsy instrument, suction biopsy instrument, gastro-urology biopsy needle and needle set, and nonelectric biopsy forceps. This section does not apply to biopsy instruments that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations. |
• Sterilization Wrap Containers (FDA Code: KCT / 880.6850) A sterilization wrap (pack, sterilization wrapper, bag, or accessories, is a device intended to be used to enclose another medical device that is to be sterilized by a health care provider. It is intended to allow sterilization of the enclosed medical device and also to maintain sterility of the enclosed device until used. |