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Standard Specifications and Test Methods for Components Used in the Surgical Fixation of the Spinal Skeletal System
Automaticky preložený názov:
Štandardné Špecifikácie a skúšobné metódy na komponenty použité na chirurgické fixácie chrbtice kostrového systému
NORMA vydaná dňa 15.11.2007
Označenie normy: ASTM F2193-02(2007)
Poznámka: NEPLATNÁ
Dátum vydania normy: 15.11.2007
Kód tovaru: NS-53131
Počet strán: 14
Približná hmotnosť: 42 g (0.09 libier)
Krajina: Americká technická norma
Kategória: Technické normy ASTM
Keywords:
bend testing-plate, bend testing-rod, bend testing-screw, bend testing-surgical implants, fatigue test-plate, fatigue test-rod, fatigue test-screw, fatigue test-surgical implants, orthopedic medical device-plate, orthopedic medical device-rod, orthopedic medical device-screw, orthopedic spinal devices, performance, spinal arthrodesis, surgical devices, terminology, test methods-surgical implants, ICS Number Code 11.040.40 (Implants for surgery, prothetics and orthotics)
1. Scope | ||||||||||||||||||||||||||||||||||||||||||||||||||
1.1 These specifications and test methods are intended to provide a comprehensive reference for the components of systems used in the surgical fixation of the spinal skeletal system. The document catalogs standard specifications that specify material, labeling, and handling requirements. The specifications and test methods also establish common terminology that can be used to describe the size and other physical characteristics of spinal components and performance definitions related to the performance of spinal components. Additionally, the specifications and test methods establish performance requirements and standard test methods to consistently measure performance-related mechanical characteristics of spinal components. 1.2 These specifications and test methods are a series of standards available for addressing the concerns related to systems used in the surgical fixation of the spinal skeletal system. These specifications and test methods concentrate on the individual components, which are found in many spinal fixation systems. If the user is interested in evaluating the next level in the spinal fixation system chain, the interconnections between individual components and subassemblies (two or more components), the user should consult Guide F 1798. At the highest level in this chain is Test Methods F 1717, which is used to evaluate an entire construct assembled from many components and involves numerous interconnections and several subassemblies. 1.3 It is not the intention of these specifications and test methods to define levels of performance or case-specific clinical performance for spinal components addressed by this document. Insufficient knowledge is available to predict the consequences of using any of these components in individual patients for specific activities of daily living. Furthermore, it is not the intention of this document to describe or specify specific designs for the individual components of systems used in the surgical internal fixation of the spinal skeletal system. 1.4 These specifications and test methods may not be appropriate for all types of spinal surgical fixation systems. The user is cautioned to consider the appropriateness of this document in view of the particular implant system and its potential application. 1.5 This document includes the following specifications and test methods that are used in determining the spinal component's mechanical performance characteristics: 1.5.1 Specification for Metallic Spinal Screws—Annex A1. 1.5.2 Specification for Metallic Spinal Plates—Annex A2. 1.5.3 Specification for Metallic Spinal Rods—Annex A3. 1.5.4 Test Method for Measuring the Static and Fatigue Bending Strength of Metallic Spinal Screws—Annex A4. 1.6 Unless otherwise indicated, the values stated in SI units shall be regarded as the standard. 1.7 This standard may involve hazardous materials, operations, and equipment. 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. |
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2. Referenced Documents | ||||||||||||||||||||||||||||||||||||||||||||||||||
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