Part B: Supplementary Information Sheet (SIS) |
FR Recognition List Number
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057
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Date of Entry 12/20/2021
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FR Recognition Number
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11-386
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Standard | |
ASTM F2665-21 Standard Specification for Total Ankle Replacement Prosthesis |
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Scope/Abstract1.1 This specification covers total ankle replacement (TAR) prostheses used to provide functioning articulation by employing talar and tibial components that allow for a minimum of 15° of dorsiflexion and 15 to 25° (1)2 of plantar flexion, as determined by non-clinical testing.
1.2 Included within the scope of this specification are ankle components for primary and revision surgery with modular and non-modular designs, bearing components with fixed or mobile bearing designs, and components for cemented and/or cementless use.
1.3 This specification is intended to provide basic descriptions of material and prosthesis geometry. In addition, those characteristics determined to be important to the in-vivo performance of the prosthesis are defined. |
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Extent of Recognition
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Rationale for Recognition
This standard is relevant to medical devices and is recognized on its scientific and technical merit and/or because it supports existing regulatory policies. |
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Public Law, CFR Citation(s) and Procode(s)*
Regulation Number |
Device Name |
Device Class |
Product Code |
§888.3100 |
Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Composite
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Class 2
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KMD
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§888.3110 |
Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer
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Class 2
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HSN
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§888.3120 |
Prosthesis, Ankle, Cemented, Non-Constrained
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Class 3
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KXC
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N/A |
Prosthesis, Ankle, Uncemented, Non-Constrained |
Class 3
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NTG
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Relevant FDA Guidance and/or Supportive Publications*
Appropriate Use of Voluntary Consensus Standards in Premarket Submissions for Medical Devices - Guidance for Industry and Food and Drug Administration Staff, issued September 2018. |
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FDA Technical Contact
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Standards Development Organization
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FDA Specialty Task Group (STG)
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*These are provided as examples and others may be applicable. |