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ASTM F382-14

Standard Specification and Test Method for Metallic Bone Plates

Automaticky preložený názov:

Štandardné špecifikácie a skúšobné metódy pre kovové platničky

NORMA vydaná dňa 1.11.2014

Jazyk
Prevedenie	PDF - okamžité stiahnutie - 83.40 € Tlačené - 83.40 €
Dostupnosť	SKLADOM
Cena	83.40 € bez DPH
83.40 €

Informácie o norme:

Označenie normy: ASTM F382-14
Poznámka: NEPLATNÁ
Dátum vydania normy: 1.11.2014
Kód tovaru: NS-55109
Počet strán: 13
Približná hmotnosť: 39 g (0.09 libier)
Krajina: Americká technická norma
Kategória: Technické normy ASTM

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Kategórie - podobné normy:

Implantáty pro chirurgii, protetiku a ortotiku

Anotácia textu normy ASTM F382-14 :

Keywords:

bend testing&mdash,surgical implants, fatigue test, bone plate, orthopedic medical devices&mdash,bone plates, surgical devices, test methods&mdash,surgical implants,, ICS Number Code 11.040.40 (Implants for surgery, prothetics and orthotics)

Doplňujúce informácie

Significance and Use

A2.5 Significance and Use

A2.5.1 This test method establishes a uniform four-point bending fatigue test to characterize and compare the fatigue performance of different bone plate designs. This test method may be used to determine a fatigue life of the bone plate at either a specific maximum bending moment or over a range of maximum bending moment conditions. Alternatively, the test method may be used to estimate a bone plate's fatigue strength for a specified number of fatigue cycles.

A2.5.2 This test method utilizes a simplified bone plate load model that may not be exactly representative of the in-situ loading configuration. The user should note that the test results generated by this test method can not be used to directly predict the in vivo performance of the bone plate being tested. The data generated from this test method can be used to conduct relative comparisons of different bone plate designs.

A2.5.3 This test method may not be appropriate for all types of implant applications. The user is cautioned to consider the appropriateness of the method in view of the devices being tested and their potential application.

A2.5.4 This test method assumes that the bone plate is manufactured from a material that exhibits linear-elastic material behavior. Therefore, the method is not applicable for testing bone plates made from materials that exhibit non-linear elastic behavior.

A2.5.5 This test method is restricted to the testing of bone plates within the lnear-elastic range of the material. . Therefore, the test method is not applicable for testing bone plates under conditions that would approach or exceed the bending strength of the bone plate being tested.

1. Scope

1.1 This specification and test method is intended to provide a comprehensive reference for bone plates used in the surgical internal fixation of the skeletal system. The standard establishes consistent methods to classify and define the geometric and performance characteristics of bone plates. The standard also presents a catalog of standard specifications that specify material; labeling and handling requirements; and standard test methods for measuring performance related mechanical characteristics determined to be important to the in vivo performance of bone plates.

1.2 It is not the intention of the standard to define levels of performance or case-specific clinical performance for bone plates, as insufficient knowledge is available to predict the consequences or their use in individual patients for specific activities of daily living. Futhermore, it is not the intention of the standard to describe or specify specific designs for bone plates used in the surgical internal fixation of the skeletal system.

1.3 This document may not be appropriate for all types of bone plates. The user is cautioned to consider the appropriateness of the standard in view of a particular bone plate and its potential application.

1.4 This document includes the following test methods used in determining the following bone plate mechanical performance characteristics:

1.4.1 Standard Test Method for Single Cycle Bend Testing of Metallic Bone Plates—Annex A1, and

1.4.2 Standard Test Method for Determining the Bending Fatigue Properties Of Metallic Bone Plates—Annex A2.

1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.

1.6 Multiple test methods are included in this standard. However, it must be noted that the user is not obligated to test using all of the described methods. Instead, the user should only select test methods that are appropriate for a particular device design. In most instances, only a subset of the herein described test methods will be required.

1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

2. Referenced Documents

ISO?14602	Non-active surgical implants--Implants for Osteosynthesis particular requirements.
E1942-98(2018)e1	Standard Guide for Evaluating Data Acquisition Systems Used in Cyclic Fatigue and Fracture Mechanics Testing (Includes all amendments and changes 8/14/2018).
F565-21	Standard Practice for Care and Handling of Orthopedic Implants and Instruments
E1823-23	Standard Terminology Relating to Fatigue and Fracture Testing
E467-21	Standard Practice for Verification of Constant Amplitude Dynamic Forces in an Axial Fatigue Testing System
E4-21	Standard Practices for Force Calibration and Verification of Testing Machines
F1713-08(2021)e1	Standard Specification for Wrought Titanium-13Niobium-13Zirconium Alloy for Surgical Implant Applications (UNS R58130) (Includes all amendments and changes 12/8/2021).
F1472-23	Standard Specification for Wrought Titanium-6Aluminum-4Vanadium Alloy for Surgical Implant Applications (UNS R56400)
ISO 9585	Implants for Surgery--Determination of Bending Strength and Stiffness of Bone Plates
F1314-18	Standard Specification for Wrought Nitrogen Strengthened 22 Chromium-13 Nickel-5 Manganese-2.5 Molybdenum Stainless Steel Alloy Bar and Wire for Surgical Implants (UNS S20910)
F1295-23	Standard Specification for Wrought Titanium-6Aluminum-7Niobium Alloy for Surgical Implant Applications (UNS R56700)
F983-86(2018)	Standard Practice for Permanent Marking of Orthopaedic Implant Components
F621-12(2021)e1	Standard Specification for Stainless Steel Forgings for Surgical Implants (Includes all amendments and changes 8/19/2021).
F620-20	Standard Specification for Titanium Alloy Forgings for Surgical Implants in the Alpha Plus Beta Condition
F565-21	Standard Practice for Care and Handling of Orthopedic Implants and Instruments
F543-23	Standard Specification and Test Methods for Metallic Medical Bone Screws
F139-19	Standard Specification for Wrought 18Chromium-14Nickel-2.5Molybdenum Stainless Steel Sheet and Strip for Surgical Implants (UNS S31673)
F138-19	Standard Specification for Wrought 18Chromium-14Nickel-2.5Molybdenum Stainless Steel Bar and Wire for Surgical Implants (UNS S31673)
F136-13(2021)e1	Standard Specification for Wrought Titanium-6Aluminum-4Vanadium ELI (Extra Low Interstitial) Alloy for Surgical Implant Applications (UNS R56401) (Includes all amendments and changes 8/19/2021).
F90-23	Standard Specification for Wrought Cobalt-20Chromium-15Tungsten-10Nickel Alloy for Surgical Implant Applications (UNS R30605)
F86-21	Standard Practice for Surface Preparation and Marking of Metallic Surgical Implants
F75-23	Standard Specification for Cobalt-28 Chromium-6 Molybdenum Alloy Castings and Casting Alloy for Surgical Implants (UNS R30075)
F67-13(2017)	Standard Specification for Unalloyed Titanium, for Surgical Implant Applications (UNS R50250, UNS R50400, UNS R50550, UNS R50700)
E122-17(2022)	Standard Practice for Calculating Sample Size to Estimate, With Specified Precision, the Average for a Characteristic of a Lot or Process

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