FDA Denies Wright Medical Group's Augment Bone Graft as Autograft Alternative

Spinal Tech

The U.S. Food and Drug Administration has denied Arlington, Tenn.-based Wright Medical Group's application to use the Augment Bone Graft for an alternative to autografts in foot and ankle fusions, according to a Daily News report. The agency's reasoning included the patient population for the trial, which the FDA said was low-risk and may not have truly needed an autograft or the Augment Bone Graft. In order to receive approval in the future, Wright Medical will need to prove patients in the trial are high-risk, according to the report.

More Articles on Devices:

Medtronic Acquires Cardiocom Disease Management Company for $200M
RTI Surgical’s Biologic Bone Graft Implanted in First Human Subject
SBi Launches Charcot Foot Solutions Website

Copyright © 2024 Becker's Healthcare. All Rights Reserved. Privacy Policy. Cookie Policy. Linking and Reprinting Policy.

 

Articles We Think You'll Like

 

Featured Webinars

Featured Whitepapers