Medical Device Manufacturer · US , Fort Wayne , IN

Vivorte, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2013
4
Total
4
Cleared
0
Denied

FDA 510(k) Regulatory Record - Vivorte, Inc. Orthopedic ✕

4 devices
1-4 of 4
Cleared Jan 14, 2015
Vivorte Trabexus EB
K143547 · MBP
Orthopedic · 30d
Cleared Jan 14, 2015
Vivorte Trabexus
K143549 · MQV
Orthopedic · 30d
Cleared Sep 12, 2013
VIVORTE BVF
K130703 · MBP
Orthopedic · 181d
Cleared Aug 12, 2013
VIVORTE BVF LITE
K131133 · MQV
Orthopedic · 111d
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