Medical Device Manufacturer · US , Andover , MN

Vertebral Technologies, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2008
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
1-7 of 7
Cleared Sep 03, 2013
INTERFUSE L INTERVERTEBRAL BODY FUSION DEVICE
K131540 · MAX
Orthopedic · 97d
Cleared May 27, 2011
INTERFUSE T INVERTEBRAL BODY FUSION DEVICE
K110226 · MAX
Orthopedic · 122d
Cleared Feb 03, 2011
INTERFUSE DA INVERTEBRAL BODY FUSION DEVICE
K110045 · MAX
Orthopedic · 28d
Cleared Oct 06, 2010
INTERFUSE T INVERTEBRAL BODY FUSION DEVICE
K102277 · MAX
Orthopedic · 56d
Cleared Dec 23, 2009
INTERFUSE INVERTEBRAL BODY FUSION DEVICE MODEL 9076
K093675 · MAX
Orthopedic · 26d
Cleared Jul 30, 2009
MODIFICATION TO: INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE , MODEL 9076
K091988 · MAX
Orthopedic · 28d
Cleared Jun 10, 2008
INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE
K080673 · MAX
Orthopedic · 92d
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