Registrar Corp

HomeMedical DevicesMedical Devices Master Files (MAF)MAF Examples › Articular Surface Replacement

Filing a MAF for Articular Surface Replacement with the U.S. FDA


Filing a medical device master file (MAF) for Articular Surface Replacement can be a useful mechanism to market your Articular Surface Replacement to the U.S. Medical Device Industry. Typical Articular Surface Replacement producers who have filed a MAF for Articular Surface Replacement include:

  - DEPUY INC.

Registrar Corp can help you to properly prepare and submit your Articular Surface Replacement MAF to FDA.

As your Agent, Registrar Corp will perform the following administrative functions:

  - Ensure administrative accuracy of your Articular Surface Replacement MAF
  - Format, assemble and deliver your Articular Surface Replacement MAF to FDA
  - Assist with preparing letters of authorization regarding your Articular Surface Replacement MAF
 - Provide changes, additions and maintenance of your Articular Surface Replacement MAF
  - Respond to issues relating to ownership of your Articular Surface Replacement MAF
  - Assist with submission of responses to FDA concerning your Articular Surface Replacement MAF

For more information about filing a MAF for Articular Surface Replacement, simply click below:




Live Help

 
U.S. FDA Regulations:

U.S. FDA 510(k) Regulation: 21 C.F.R. section 814.9.


Registrar Corp assists businesses with U.S. FDA compliance. Certificates of Registration issued by Registrar Corp provide confirmation to industry that you are fulfilling U.S. FDA registration requirements. U.S. FDA does not issue or recognize Certificates of Registration. Registrar Corp is not affiliated with the U.S. Food and Drug Administration.
Home | About Us | News | Resources | Exhibitions | Seminars | Associations | Careers | Sitemap | Terms of Use © 2016 Registrar Corp
 
Food and Beverages | Drugs | Cosmetics | Medical Devices | Radiation-Emitting Electronic Devices | Color Additives | Tobacco