Adaptive Specialty, LLC is one of 20241 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Adaptive Specialty, LLC - FDA 510(k) Cleared Devices
Recent clearances: ADAPTIVE WEDGE, FUSION ADVANTAGE CERVICAL CAGE, FUSION ADVANTAGE LUMBAR CAGE
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