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FDA 510(k) Applications Submitted by VERTEBRAL TECHNOLOGIES, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K080673
03/10/2008
INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE
VERTEBRAL TECHNOLOGIES, INC.
K110045
01/06/2011
INTERFUSE DA INVERTEBRAL BODY FUSION DEVICE
VERTEBRAL TECHNOLOGIES, INC.
K110226
01/25/2011
INTERFUSE T INVERTEBRAL BODY FUSION DEVICE
VERTEBRAL TECHNOLOGIES, INC.
K131540
05/29/2013
INTERFUSE L INTERVERTEBRAL BODY FUSION DEVICE
VERTEBRAL TECHNOLOGIES, INC.
K091988
07/02/2009
MODIFICATION TO: INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE , MODEL 9076
VERTEBRAL TECHNOLOGIES, INC.
K102277
08/11/2010
INTERFUSE T INVERTEBRAL BODY FUSION DEVICE
VERTEBRAL TECHNOLOGIES, INC.
K093675
11/27/2009
INTERFUSE INVERTEBRAL BODY FUSION DEVICE MODEL 9076
VERTEBRAL TECHNOLOGIES, INC.
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