Cartiva, Inc. is one of 19947 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cartiva, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Cartiva SCI instrumentation set, Cartiva SCI Disposable Instrumentation Set, ProxiFuse Hammer Toe Device
3
Total
3
Cleared
0
Denied
Cartiva, Inc. has 3 FDA 510(k) cleared medical devices. Based in Alpharetta, US.
Historical record: 3 cleared submissions from 2014 to 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Cartiva, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory and Clinical Research Institute as regulatory consultant.
FDA 510(k) Regulatory Record - Cartiva, Inc.
3 devices