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ASTM F2083-06b
Standard Specification for Total Knee Prosthesis (Includes all amendments And changes 8/16/2017).
Automatische name übersetzung:
Standard-Spezifikation für Gesamtknieprothese
NORM herausgegeben am 1.9.2006
Informationen über die Norm:
Bezeichnung normen: ASTM F2083-06b
Anmerkung: UNGÜLTIG
Ausgabedatum normen: 1.9.2006
SKU: NS-52730
Zahl der Seiten: 7
Gewicht ca.: 21 g (0.05 Pfund)
Land: Amerikanische technische Norm
Kategorie: Technische Normen ASTM
Die Annotation des Normtextes ASTM F2083-06b :
Keywords:
arthroplasty, contact area, contact pressure, fatigue, knee, knee constraint, knee prosthesis, knee wear, particles, surface roughness, total knee replacement, TKR, UHMWPE, ICS Number Code 11.040.40 (Implants for surgery, prothetics and orthotics)
Ergänzende Informationen
| 1. Scope | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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1.1 This specification covers total knee replacement (TKR) prostheses used to provide functioning articulation by employing femoral and tibial components, allowing a minimum of 110 of flexion to high flexion. Although a patellar component may be considered an integral part of a TKR, the detailed description of this component is excluded here since it is provided in Specification F 1672. 1.2 Included within the scope of this specification are replaceable components of modular designs, for example, tibial articulating surfaces and all components labeled for or capable of being used with cement, regardless of whether the same components can also be used without cement. This includes primary and revision prostheses and also covers fixed and mobile bearing knee designs. 1.3 This specification is intended to provide basic descriptions of material and prosthesis geometry. Additionally, those characteristics determined to be important to in vivo performance of the prosthesis are defined. 1.4 Excluded from the scope are hemiarthroplasty devices that replace only the femoral or tibial surface, but not both; unicompartmental designs, which replace the articulating surfaces of only one condyle; and patellofemoral prostheses. Also excluded are devices designed for custom applications. |
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| 2. Referenced Documents | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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