Additive Manufacturing
Mechanical Test Methods for Medical Devices
Andrew Smith, PE
Manager, Joint Arthroplasty
Element Materials Technology
Overview
• Company Introduction and Background
• Areas of Additive Manufacturing Evaluation
• Mechanical Testing Methods
• General
• Medical-specific
• Strategies for Protocol Development
• Common Pitfalls to Avoid
Company Introduction and Background
• Element is a global platform of laboratories with 200+
locations around the world.
• We specialize in material testing and product qualification
testing across several major industries.
• Aerospace
• Energy
• Ground Transportation
• Building Products
• Pharmaceuticals
• Medical Device
• Orthopedic
• Cardiovascular
• Other implantable devices
Test Requirements - Guiding Organizations
• Regulatory Bodies
• FDA
• European Commission / Notified Bodies
• PMDA
• Standardization Organizations
• ASTM International
• F42, F04
• International Organization for Standardization (ISO)
• TC261, TC150
Areas of Consideration for Additive Manufacturing Evaluation
• Raw Material Chemistry
• Powder Morphology
• Process Consistency
• Build Orientation and Location
• Biocompatibility
• Cleanliness
• Sterilization
• Sintering / Particle Shedding
• Mechanical Properties
• Static
• Fatigue
• Tribology
General Mechanical Testing Methods – Material Characterization
• ASTM E8 Tensile Testing
• ASTM E9 Compression Testing
• ASTM F1160 / ISO 1143 Rotating Beam Fatigue Testing
• ASTM E647 Fatigue Crack Growth
• ASTM E399 Fracture Toughness
• ASTM E1820 Fracture Toughness
Medical-Specific Test Methods
• Modified Surfaces / Porous Structures
• Component level static and fatigue testing
• Coupon and component level wear testing
• FDA Guidance Document
• Technical Considerations for Additive Manufactured Medical Devices
Component Fatigue Testing
• The scopes of existing test standards encompass implants
made using a variety of manufacturing processes.
• As such, AM implants are covered and should be
tested under current standards.
• AM devices are not exempt from minimum performance requirements.
• AM devices may be subject to additional test requirements if designs
are deemed sensitive to other failure modes.
• Additional fatigue testing on components such as:
• Acetabular Shells
• Femoral Components
Modified Surfaces / Porous Structures
• Several published test methods and standards:
• ASTM F1044, F1147, F1160 Tensile and Shear
• ASTM F1160 / ISO 1143 Rotating Beam and Bending Fatigue
• ASTM F1978 Taber Abrasion
• ASTM F1854 Stereoscopic Examination
• ASTM F2077 Compression Testing
• In general, reference FDA guidance documents:
• Guidance for Industry on the Testing of Metallic Plasma Sprayed Coatings on Orthopedic
Implants to Support Reconsideration of Postmarket Surveillance Requirements
• Guidance Document for Testing Orthopedic Implants With Modified
Metallic Surfaces Apposing Bone Or Bone Cement
ASTM F1044, F1147, F1160 Tensile and Shear
• Standard mechanical strength evaluation for “coatings”
• Coupon with porous structure surface glued to blank coupon
• F1044 Static Shear and F1147 Static Tensile have recommended
performance requirements listed in FDA guidance documents
• F1044 – tensile strength >22 MPa
• F1147 – shear strength >20 MPa
• F1160 requires generating a fatigue curve and determining
the maximum stress level that survives 10M cycles
• Challenges
• AM specimens are often weaker than other coatings
• Characterizing effects from build location / orientation
ASTM F1044, F1147, F1160 Tensile and Shear
• Specimen prep, gluing, and alignment are critical!
• Statics are often tested with 5 to 6 specimens
• F1160 dynamic shear
• Only 6 specimens often required for other manufacturing methods
• Test 8 to 10 AM specimens due to increased scatter in results
• Recommend building extra specimens to prevent delays in testing
ASTM F1160 / ISO 1143 Rotating Beam and Bending Fatigue
• Used to evaluate the effects of surface modification / coating
on base material bending fatigue properties
• Rotating beam fatigue allows for high frequency testing (50Hz)
• Specimen concentricity is critical, but can be difficult to
achieve with AM processes
• Flat 4-point bend specimens can be easier to
fabricate, but flatness is still important
• Fatigue Strength > 130 Mpa
• Test at least 10 specimens
ASTM F1978 Taber Abrasion
• Standard abrasion test for “coatings”
• Coupons need to be flat!
• Large build dimensions can lead to warping
• Recommended performance requirements listed in FDA
guidance: 65 mg maximum loss over 100 cycles
• AM coupons have a tendency to exhibit particle shedding
• Make sure residual material has been removed prior to test
• Modified cleaning methods may be necessary to
release trapped particles
• 7 specimens required
ASTM F1854 Stereoscopic Examination
• Provide characterization of porosity, coating thickness,
and spacing between structures
• Additionally the method can provide insight into strut porosity,
level of sintering, and existence of residual powder
• Additional cross-sectional area beyond what is required by the specification
is needed to adequately characterize non-uniform structures
• Digital imaging and computerized processing methods are needed
to properly evaluate and characterize structures
ASTM F2077 Compression and Compression Shear
• Provide stiffness and other macro-level mechanical
properties for complex strut structures.
• Can be used for lot validation or characterization
of build location and orientation.
• Adequate sample size should be used based on
variability of porous / strut structure.
Tribology
• AM materials generally include higher
levels of porosity and inclusions and
feature anisotropic structure.
• This can play a role in wear performance
on articulating surfaces.
• AM materials may also perform differently
in abrasive / 3rd body wear conditions
• Material / process screen can be performed
using ASTM G99 and ASTM F732
Pin on Disk Testing
• Component level testing should follow.
Protocol Development Strategies
• Consider the purpose of the testing and review applicable requirements
• Consult guidance documents and test standards
• Check for draft standards and work items as these may include more
up-to-date information
• Resolve conflicting requirements
• Detail test method and specimen preparation as much as possible
• Set acceptance criteria including acceptable and unacceptable results
and behaviors
• Consider statistical requirements to determine appropriate sample size
and how you will analyze the numerical data
• Review protocol with suppliers and testing partners prior to approval
Common Mistakes to Avoid
• Not addressing particle shedding / residual material
• Creating too few test specimens
• Fabrication of test coupons that are out of concentricity, or
that warp during post-processing
• Setting acceptance criteria that are too high (e.g. comparing
fatigue strength to conventional materials)
• Failing to set any acceptance criteria prior to start of testing
• Not accounting for build orientation
• Inconsistent test sample preparation / gluing / alignment
Additive Manufacturing - Mechanical Test Methods - OMTEC 2018

Additive Manufacturing - Mechanical Test Methods - OMTEC 2018

  • 2.
    Additive Manufacturing Mechanical TestMethods for Medical Devices Andrew Smith, PE Manager, Joint Arthroplasty Element Materials Technology
  • 3.
    Overview • Company Introductionand Background • Areas of Additive Manufacturing Evaluation • Mechanical Testing Methods • General • Medical-specific • Strategies for Protocol Development • Common Pitfalls to Avoid
  • 4.
    Company Introduction andBackground • Element is a global platform of laboratories with 200+ locations around the world. • We specialize in material testing and product qualification testing across several major industries. • Aerospace • Energy • Ground Transportation • Building Products • Pharmaceuticals • Medical Device • Orthopedic • Cardiovascular • Other implantable devices
  • 5.
    Test Requirements -Guiding Organizations • Regulatory Bodies • FDA • European Commission / Notified Bodies • PMDA • Standardization Organizations • ASTM International • F42, F04 • International Organization for Standardization (ISO) • TC261, TC150
  • 6.
    Areas of Considerationfor Additive Manufacturing Evaluation • Raw Material Chemistry • Powder Morphology • Process Consistency • Build Orientation and Location • Biocompatibility • Cleanliness • Sterilization • Sintering / Particle Shedding • Mechanical Properties • Static • Fatigue • Tribology
  • 7.
    General Mechanical TestingMethods – Material Characterization • ASTM E8 Tensile Testing • ASTM E9 Compression Testing • ASTM F1160 / ISO 1143 Rotating Beam Fatigue Testing • ASTM E647 Fatigue Crack Growth • ASTM E399 Fracture Toughness • ASTM E1820 Fracture Toughness
  • 8.
    Medical-Specific Test Methods •Modified Surfaces / Porous Structures • Component level static and fatigue testing • Coupon and component level wear testing • FDA Guidance Document • Technical Considerations for Additive Manufactured Medical Devices
  • 9.
    Component Fatigue Testing •The scopes of existing test standards encompass implants made using a variety of manufacturing processes. • As such, AM implants are covered and should be tested under current standards. • AM devices are not exempt from minimum performance requirements. • AM devices may be subject to additional test requirements if designs are deemed sensitive to other failure modes. • Additional fatigue testing on components such as: • Acetabular Shells • Femoral Components
  • 10.
    Modified Surfaces /Porous Structures • Several published test methods and standards: • ASTM F1044, F1147, F1160 Tensile and Shear • ASTM F1160 / ISO 1143 Rotating Beam and Bending Fatigue • ASTM F1978 Taber Abrasion • ASTM F1854 Stereoscopic Examination • ASTM F2077 Compression Testing • In general, reference FDA guidance documents: • Guidance for Industry on the Testing of Metallic Plasma Sprayed Coatings on Orthopedic Implants to Support Reconsideration of Postmarket Surveillance Requirements • Guidance Document for Testing Orthopedic Implants With Modified Metallic Surfaces Apposing Bone Or Bone Cement
  • 11.
    ASTM F1044, F1147,F1160 Tensile and Shear • Standard mechanical strength evaluation for “coatings” • Coupon with porous structure surface glued to blank coupon • F1044 Static Shear and F1147 Static Tensile have recommended performance requirements listed in FDA guidance documents • F1044 – tensile strength >22 MPa • F1147 – shear strength >20 MPa • F1160 requires generating a fatigue curve and determining the maximum stress level that survives 10M cycles • Challenges • AM specimens are often weaker than other coatings • Characterizing effects from build location / orientation
  • 12.
    ASTM F1044, F1147,F1160 Tensile and Shear • Specimen prep, gluing, and alignment are critical! • Statics are often tested with 5 to 6 specimens • F1160 dynamic shear • Only 6 specimens often required for other manufacturing methods • Test 8 to 10 AM specimens due to increased scatter in results • Recommend building extra specimens to prevent delays in testing
  • 13.
    ASTM F1160 /ISO 1143 Rotating Beam and Bending Fatigue • Used to evaluate the effects of surface modification / coating on base material bending fatigue properties • Rotating beam fatigue allows for high frequency testing (50Hz) • Specimen concentricity is critical, but can be difficult to achieve with AM processes • Flat 4-point bend specimens can be easier to fabricate, but flatness is still important • Fatigue Strength > 130 Mpa • Test at least 10 specimens
  • 14.
    ASTM F1978 TaberAbrasion • Standard abrasion test for “coatings” • Coupons need to be flat! • Large build dimensions can lead to warping • Recommended performance requirements listed in FDA guidance: 65 mg maximum loss over 100 cycles • AM coupons have a tendency to exhibit particle shedding • Make sure residual material has been removed prior to test • Modified cleaning methods may be necessary to release trapped particles • 7 specimens required
  • 15.
    ASTM F1854 StereoscopicExamination • Provide characterization of porosity, coating thickness, and spacing between structures • Additionally the method can provide insight into strut porosity, level of sintering, and existence of residual powder • Additional cross-sectional area beyond what is required by the specification is needed to adequately characterize non-uniform structures • Digital imaging and computerized processing methods are needed to properly evaluate and characterize structures
  • 16.
    ASTM F2077 Compressionand Compression Shear • Provide stiffness and other macro-level mechanical properties for complex strut structures. • Can be used for lot validation or characterization of build location and orientation. • Adequate sample size should be used based on variability of porous / strut structure.
  • 17.
    Tribology • AM materialsgenerally include higher levels of porosity and inclusions and feature anisotropic structure. • This can play a role in wear performance on articulating surfaces. • AM materials may also perform differently in abrasive / 3rd body wear conditions • Material / process screen can be performed using ASTM G99 and ASTM F732 Pin on Disk Testing • Component level testing should follow.
  • 18.
    Protocol Development Strategies •Consider the purpose of the testing and review applicable requirements • Consult guidance documents and test standards • Check for draft standards and work items as these may include more up-to-date information • Resolve conflicting requirements • Detail test method and specimen preparation as much as possible • Set acceptance criteria including acceptable and unacceptable results and behaviors • Consider statistical requirements to determine appropriate sample size and how you will analyze the numerical data • Review protocol with suppliers and testing partners prior to approval
  • 19.
    Common Mistakes toAvoid • Not addressing particle shedding / residual material • Creating too few test specimens • Fabrication of test coupons that are out of concentricity, or that warp during post-processing • Setting acceptance criteria that are too high (e.g. comparing fatigue strength to conventional materials) • Failing to set any acceptance criteria prior to start of testing • Not accounting for build orientation • Inconsistent test sample preparation / gluing / alignment