Calvary Spine, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Calvary Spine, LLC - FDA 510(k) Cleared Devices
Recent clearances: Calvary Spine Pedicle Screw System
2
Total
2
Cleared
0
Denied
Calvary Spine, LLC has 2 FDA 510(k) cleared medical devices. Based in Round Rock, US.
Historical record: 2 cleared submissions from 2008 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Calvary Spine, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by The OrthoMedix Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Calvary Spine, LLC
2 devices