ASTM F382-1999(2003)e1 Standard Specification and Test Method for Metallic Bone Plates《金属骨板的静态弯曲特性的测试方法和标准规范》.pdf
《ASTM F382-1999(2003)e1 Standard Specification and Test Method for Metallic Bone Plates《金属骨板的静态弯曲特性的测试方法和标准规范》.pdf》由会员分享,可在线阅读,更多相关《ASTM F382-1999(2003)e1 Standard Specification and Test Method for Metallic Bone Plates《金属骨板的静态弯曲特性的测试方法和标准规范》.pdf(12页珍藏版)》请在麦多课文档分享上搜索。
1、Designation: F 382 99 (Reapproved 2003)e1Standard Specification and Test Method forMetallic Bone Plates1This standard is issued under the fixed designation F 382; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of last rev
2、ision. A number in parentheses indicates the year of last reapproval. Asuperscript epsilon (e) indicates an editorial change since the last revision or reapproval.e1NOTEEditorial changes were made throughout in December 2004.1. Scope1.1 This specification and test method is intended to providea comp
3、rehensive reference for bone plates used in the surgicalinternal fixation of the skeletal system. The standard estab-lishes consistent methods to classify, define the geometriccharacteristics, and performance characteristics of bone plates.The standard also presents a catalog of standard specificati
4、onsthat specify material; labeling and handling requirements; andstandard test methods for measuring performance relatedmechanical characteristics determined to be important to the invivo performance of bone plates.1.2 It is not the intention of the standard to define levels ofperformance or case-sp
5、ecific clinical performance for boneplates, as insufficient knowledge is available to predict theconsequences or their use in individual patients for specificactivities of daily living. Futhermore, it is not the intention ofthe standard to describe or specify specific designs for boneplates used in
6、the surgical internal fixation of the skeletalsystem.1.3 This document may not be appropriate for all types ofbone plates. The user is cautioned to consider the appropriate-ness of the standard in view of a particular bone plate and itspotential application.1.4 This document includes the following t
7、est methods usedin determining the following bone plate mechanical perfor-mance characteristics.1.4.1 Standard Test Method for Single Cycle Bend Testingof Metallic Bone PlatesAnnex A1.1.4.2 Standard Test Method for Determining the BendingFatigue Properties Of Metallic Bone PlatesAnnex A2.1.5 Unless
8、otherwise indicated, the values stated in SI unitsshall be regarded as the standard.1.6 This standard does not purport to address all of thesafety concerns, if any, associated with its use. It is theresponsibility of the user of this standard to establish appro-priate safety and health practices and
9、 determine the applica-bility of regulatory limitations prior to use.2. Referenced Documents2.1 ASTM Standards:2F 67 Specification for Unalloyed Titanium for SurgicalImplant ApplicationsF 75 Specification for Cobalt-28 Chromium-6 MolybdenumAlloy Castings and Casting Alloy for Surgical Implants(UNS R
10、30075)F 86 Practice for Surface Preparation and Marking of Me-tallic Surgical ImplantsF 90 Specification for Wrought Cobalt-20Chromium-15Tungsten-10Nickel Alloy for Surgical Implant Applica-tions (UNS R56401)F 136 Specification for Wrought Titanium-6Aluminum-4Vanadium ELI (Extra Low Interstitial) Al
11、loy for SurgicalImplant Applications (UNS R56401)F 138 Specification for Wrought 18Chromium-14Nickel-2.5Molybdenum Stainless Steel Bar and Wire for SurgicalImplants (UNS S31673)F 139 Specification for Wrought 18Chromium-14Nickel-2.5Molybdenum Stainless Steel Sheet and Strip for Surgi-cal Implants (U
12、NS S31673)F 543 Specification and Test Methods for Metallic MedicalBone ScrewsF 565 Practice for Care and Handling of Orthopedic Im-plants and InstrumentsF 620 Specification for Alpha Plus Beta Titanium AlloyForgings for Surgical ImplantsF 621 Specification for Stainless Steel Forgings for SurgicalI
13、mplantsF 983 Practice for Permanent Marking of Orthopaedic Im-plant ComponentsF 1295 Specification for Wrought Titanium-6Aluminum-7Niobium Alloy for Surgical Implant ApplicationsF 1314 Wrought Nitrogen Strengthened-22Chromium-12.5Nickel-5Manganese-2.5Molybdenum Stainless SteelBar and Wire for Surgic
14、al Implants (UNS S20910)F 1472 Specification for Alpha Plus Beta Titanium Alloy1This test method is under the jurisdiction ofASTM Committee F04 on Medicaland Surgical Materials and Devices and is the direct responsibility of SubcommitteeF04.21 on Osteosynthesis.Current edition approved Apr. 10, 2003
15、. Published May 2003. Originallyapproved in 1973. Last previous edition approved in 1999 as F 382 99.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For Annual Book of ASTMStandards volume information, refer to the standards D
16、ocument Summary page onthe ASTM website.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.Forgings for Surgical ImplantsF 1713 Specification for Wrought Titanium-13Niobium-13Zirconium Alloy for Surgical Implant Applications2.2 ISO Stan
17、dard:3FDIS 14602 Non-active surgical implantsImplants forOsteosynthesis particular requirements.3. Terminology3.1 DefinitionsGeometric:3.1.1 auto compressiona type of bone plate that by itsdesign can generate a compressive force between adjacentunconnected bone fragments through the use of one or mo
18、reramped holes or another type of slot geometry. This ramp orslot geometry contacts the underside of the screw head, andinduces compressive force as the screw is inserted and tight-ened to the bone plate.3.1.2 bone platea metallic device with two or more holesor slot(s), or both, and a cross section
19、 that consists of at leasttwo dimensions (width and thickness) which generally are notthe same in magnitude. The device is intended to providealignment and fixation of two or more bone sections, primarilyby spanning the fracture or defect. The device is typically fixedto the bone through the use of
20、bone screws or cerclage wire. Apartial list of general types of bone plates is given in Section4.1.3.1.3 bone plate length, L (mm)the linear dimension ofthe bone plate measured along the longitudinal axis as illus-trated in Fig. 2.3.1.4 bone plate thickness, b (mm)the linear dimension ofthe bone pla
21、te measured parallel to the screw hole axis asshown in Fig. 1a, 1b, and Fig. 2. For a bone plate with acrescent section, the thickness is measured at the thickest pointalong the section.3.1.5 bone plate width, w (mm)the linear dimension of thebone plate measured perpendicular to both the length andt
22、hickness axes as shown in Fig. 2.3.1.6 contouringthe manipulation and bending of a boneplate, either pre-operatively or intra-operatively, to match theanatomic geometry of the intended fixation location.3.1.7 crescent sectiona bone plate cross-section shape(perpendicular to the long axis of the bone
23、 plate) where thethickness is not constant along the section. Typically thesection is thickest along the bone plates centerline and tapersto a smaller thickness at the bone plates edges (see Fig. 1b).3.1.8 uniform widthreferring to a bone plate where thewidth is constant along the bone plates length
24、.3.2 DefinitionsMechanical/Structural:3.2.1 bending stiffness, K (N/mm) of a bone plate, themaximum slope of the linear elastic portion of the load versusload-point displacement curve for a bone plate when testedaccording to the test method of Annex A1.3.2.2 bending strength (N-m) of a bone plate, t
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