Medical Device Manufacturer · US , Round Rock , TX

Kasios - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2009

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Kasios Orthopedic ✕

1 devices

1-1 of 1

Cleared Dec 01, 2009

DUOWEDGE SYNTHETIC BONE SUBSTITUTE

Orthopedic · 748d