155 Episodes

  1. The Special 510k Program

    Published: 11/13/2019
  2. Beyond 510(k)/PMA—Safer Technologies Program

    Published: 10/16/2019
  3. Benefit-Risk Determinations

    Published: 9/16/2019
  4. Mike on Medtech: Beyond 510(k)/PMA—Breakthrough Devices Program

    Published: 8/6/2019
  5. Beyond 510(k)/PMA—De Novo 101

    Published: 7/2/2019
  6. Mike on Medtech: The NYT Editorial Board Statement

    Published: 6/17/2019
  7. The Alternative Summary Reporting Program

    Published: 5/24/2019
  8. Do we need a pre-sub for 483s? (Part 2)

    Published: 5/9/2019
  9. Do we need a pre-sub for 483s?

    Published: 5/9/2019
  10. FDA's Material Evaluation

    Published: 4/2/2019
  11. 510k Modernization

    Published: 1/25/2019
  12. Personalized Healthcare

    Published: 1/3/2019
  13. My Holiday Wish List (Part 2)

    Published: 12/11/2018
  14. My Holiday Wish List (Part 1)

    Published: 12/4/2018
  15. Regulating the Practice of Medicine

    Published: 10/26/2018
  16. The Bleeding Edge, Part 3

    Published: 9/26/2018
  17. The Bleeding Edge, Part 2

    Published: 9/7/2018
  18. The Bleeding Edge, Part 1

    Published: 9/5/2018
  19. Breakthrough Designation Program

    Published: 8/10/2018
  20. 15 Tips for Getting New Products Through FDA

    Published: 7/3/2018

7 / 8

A podcast focused on the medical device technology industry, from design and development to outsourcing services and relationships to finished medtech products.