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Recognized Consensus Standards

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Recognition List Number: 026 Publication Date: 03/14/2011 

Part B: SUPPLEMENTARY INFORMATION

Recognition Number 2-170: ISO 10993-14 First edition 2001-11-15, Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics. (Biocompatibility)

Date of Standard: 2001. 
Address of Standards Organization:
  International Organization for Standardization (ISO)*
  1, Rue de Varembe
  Case Postale 56
  CH 1211 Geneva 20, 0
  SWITZERLAND
CDRH Office and Division Associated with Recognized Standards:
OFFICE OF DEVICE EVALUATION (ODE)
Devices Affected:
Total joint replacement (e.g., hip, knee, shoulder, finger, etc.)
Processes Affected:
510(k), PMA, IDE, PDP, HDE, Design Control Input, Quality System Regulation
Type of Standard:
 Horizontal, International
Extent of Recognition:
Complete standard.

This is not a performance standard. The testing proposed to meet this standard must still be reviewed and evaluation against FDA requirements for safety and efficacy.
Related CFR Citations and Product Codes:
Regulation
Number
Device Name Device
Class
Product
Code
§872.3630 Abutment, Implant, Dental, Endosseous Class 2 NHA
 
Regulation
Number
Device Name Device
Class
Product
Code
§872.3640 Implant, Endosseous, Root-Form Class 2 DZE
 
Regulation
Number
Device Name Device
Class
Product
Code
§888.3353 Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented Class 2 LZO
§888.3353 Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate Class 2 MEH
 
Relevant Guidance:
Extraction Guidance for Polymeric Materials, Chemistry Group, FDA/CDRH/OSEL/DCMS

ISO 10993-12:2007: Biological Evaluation of Medical Devices -- Part 12: Sample preparation and reference materials

For further guidance, see FDA Bluebook Memorandum G95-1 "Use of International Standard ISO 10993, 'Biological Evaluation of Medical Devices Part 1: Evaluation and Testing'."
FDA Technical Contact:
  Scott McNamee
  FDA/CDRH/OC
  10903 New Hampshire Avenue Building 66, Room 3416
  Silver Spring MD 20993
  301/796-5800
  Email: scott.mcnamee@fda.hhs.gov
* In the United States, copies of this standard can be obtained from:
  American National Standards Institute (ANSI)*
  25 West 43rd Street
  4th Floor
  New York, NY 10036
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