FDA ‘breakthrough’ status for synthetic meniscus bodes well for Memphis’ Active Implants
“Instead of going through our process and filing what we think the FDA wants from us, we enter a phase called the sprint interface,” said Ted Davis, president and CEO Active Implants, “for an ongoing review of our progress in real time. We believe it will help us be more efficient and shorten the time to work through the approval process.” (Mark Weber/Daily Memphian)
Active Implants’ president and CEO hopes to shave time off the FDA approval process for the company's synthetic meniscus device.
Topics
breakthrough device designation Dr. Tom Geil FDA Ted DavisJane Roberts
Longtime journalist Jane Roberts is a Minnesotan by birth and a Memphian by choice. She's lived and reported in the city more than two decades. She covers business news and features for The Daily Memphian.
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