Medical Device Manufacturer · US , Round Rock , TX

Adaptive Specialty, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2009
2
Total
2
Cleared
0
Denied

Adaptive Specialty, LLC has 2 FDA 510(k) cleared medical devices. Based in Round Rock, US.

Historical record: 2 cleared submissions from 2009 to 2012. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Adaptive Specialty, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Adaptive Specialty, LLC
2 devices
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