Abstract
Increased awareness of potentially detrimental outcomes following partial meniscectomy led to the development of a novel meniscal scaffold, Actifitâ„¢, by Orteq Bioengineering. It received the CE Mark in July 2008 for treatment of medial or lateral irreparable partial meniscal tears. Actifitâ„¢ consists of highly interconnected porous synthetic material enabling tissue ingrowth. Over time, transformation into meniscus-like tissue takes place as the implant slowly degrades. Furthermore, Actifitâ„¢ is made of an aliphatic polyurethane, which provides optimal mechanical strength, biocompatibility, porosity, safe degradation and ease of use required for the indication. It is available in two shapes, medial and lateral.
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Notes
- 1.
Kamerlingheplein 16, 9712 TR, Groningen, The Netherlands. e-mail:Â jenhde.groot@wxs.nl
- 2.
Department of Orthopaedics and Trauma, University Hospital, De Pintelaan 185, 9000 Gent, Belgium. e-mail: Rene.verdonk@ugent.be
- 3.
Department of orthopaedics and trauma, Monica ziekenhuizen, 2000 Antwerpen, Belgium.
- 4.
Tissue Therapies Europe Limited, Unit F34, Daresbury Innovation Centre, Keckwick Lane, Daresbury, Cheshire WA4 4FS, England. e-mail: heinrichsel@aol.com
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Verdonk, R. (2013). Polyurethane Implant (ACTIFIT). In: Verdonk, R., Espregueira Mendes, J., Monllau, J. (eds) Meniscal Transplantation. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-38106-5_7
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DOI: https://doi.org/10.1007/978-3-642-38106-5_7
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