Public Workshop Reminder: Spinal Device Premarket Review – August 13, 2020

Public Workshop Reminder: Spinal Device Premarket Review

The U.S. Food and Drug Administration (FDA) is announcing a public workshop titled Spinal Device Premarket Review. The purpose of this workshop is to share information with stakeholders including members of the orthopedic community, device manufacturers and industry consultants, on FDA issued product specific, and general guidances to improve submission quality and promote efficient review of orthopedic premarket applications. Workshop Date: Thursday, August 13 from 8 AM to 5 PM ET Location: The public workshop will be webcast live and the link will be provided in your confirmation email if you registered to view the webcast. The link for archived webcast will be posted to the webpage for viewing after the public workshop. Registration Deadline: Registration will be on a first-come, first-served basis.

Learn More and Register Important Deadline September 14, 2020: Submit written comments to the docket (FDA-2020-N-1524). Questions? If you have questions about this public workshop, contact LCDR Ogochukwu Ogoegbunam, PharmD, BCGP, RAC by email at Ogochukwu.Ogoegbunam@fda.hhs.gov.