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ASTM F2083-01a
Standard Specification for Total Knee Prosthesis (Includes all amendments And changes 8/16/2017).
Automatically translated name:
Standard Specification for Total Knee Prosthesis
STANDARD published on 10.6.2001
The information about the standard:
Designation standards: ASTM F2083-01a
Note: WITHDRAWN
Publication date standards: 10.6.2001
SKU: NS-52725
The number of pages: 7
Approximate weight : 21 g (0.05 lbs)
Country: American technical standard
Category: Technical standards ASTM
Annotation of standard text ASTM F2083-01a :
Keywords:
aarthroplasty, 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)
Additional information
| 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. 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 F1672. 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 standard 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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