Integrity Spine Lumbar Interbody Fusion System is one of 18553 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Integrity Spine Lumbar Interbody Fusion System - FDA 510(k) Cleared D...
Recent clearances: Integrity Spine Lumbar Interbody Fusion System
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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.
510(k) submissions have been managed by Kaedon Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Integrity Spine Lumbar Interbody Fusion System
1 devices