Integrity Spine Lumbar Interbody Fusion System - FDA 510(k) Cleared D...
1
Total
1
Cleared
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Denied
Integrity Spine Lumbar Interbody Fusion System has 1 FDA 510(k) cleared medical devices. Based in San Antonio, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Integrity Spine Lumbar Interbody Fusion System Filter by specialty or product code using the sidebar.
1 devices