Vertebral Technologies, Inc. is one of 19117 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vertebral Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: INTERFUSE L INTERVERTEBRAL BODY FUSION DEVICE, INTERFUSE T INVERTEBRAL BODY FUSION DEVICE, INTERFUSE DA INVERTEBRAL BODY FUSION DEVICE
7
Total
7
Cleared
0
Denied
Vertebral Technologies, Inc. has 7 FDA 510(k) cleared medical devices. Based in Andover, US.
Historical record: 7 cleared submissions from 2008 to 2013. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Vertebral Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vertebral Technologies, Inc.
7 devices
Cleared
Sep 03, 2013
INTERFUSE L INTERVERTEBRAL BODY FUSION DEVICE
Orthopedic
97d
Cleared
May 27, 2011
INTERFUSE T INVERTEBRAL BODY FUSION DEVICE
Orthopedic
122d
Cleared
Feb 03, 2011
INTERFUSE DA INVERTEBRAL BODY FUSION DEVICE
Orthopedic
28d
Cleared
Oct 06, 2010
INTERFUSE T INVERTEBRAL BODY FUSION DEVICE
Orthopedic
56d
Cleared
Dec 23, 2009
INTERFUSE INVERTEBRAL BODY FUSION DEVICE MODEL 9076
Orthopedic
26d
Cleared
Jul 30, 2009
MODIFICATION TO: INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE , MODEL 9076
Orthopedic
28d
Cleared
Jun 10, 2008
INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE
Orthopedic
92d