OsteoMed ExtremiFix Cannulated Screw System – Midsize & Large Surgical Technique

Document



Document TitleDocument TypeLanguagePublishedUpdated
OsteoMed ExtremiFix Cannulated Screw System – Midsize & Large Surgical Technique (ST-030-2025-A)Surgical TechniqueEnglish ENDecember 13, 2021December 13, 2021

The ExtremiFix Midsize I Large Cannulated Screw’s unique designed allows for controlled compression on both headed and headless screws. The headless screws can be used alone generating 2 mm of interfragmentary compression, or used in conjunction with the system’s reduction tool allowing unlimited controlled compression. Indications: The OsteoMed ExtremiFix Midsize I Large Cannulated Screw system is indicated for use in bone reconstruction, osteotomy, arthrodesis, and fracture fixation of foot, ankle, and long bones (upper and lower extremity). Contraindications: Use of the OsteoMed ExtremiFix Midsize I Large Cannulated Screw system is contraindicated in cases of active or suspected infection or in patients who are immunocompromised; in patients previously sensitized to titanium; or in patients with certain metabolic diseases. It is further contraindicated in patients exhibiting disorders which would cause the patient to ignore the physician’s pre- and/or postoperative instructions and/or the limitations of internal rigid fixation implants.