FDA 510(k) Applications Submitted by Pinnacle Spine Group, LLC
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K140066 |
01/10/2014 |
INFILL CERVICAL |
PINNACLE SPINE GROUP, LLC |
| K151184 |
05/04/2015 |
InFill Interbody Fusion Devices |
PINNACLE SPINE GROUP, LLC |
| K121476 |
05/18/2012 |
INFILL GRAFT DELIVERY SYSTEM |
PINNACLE SPINE GROUP, LLC |
| K121733 |
06/13/2012 |
INFILL INTERVERTEBRAL BODY FUSION DEVICE |
PINNACLE SPINE GROUP, LLC |
| K152259 |
08/11/2015 |
InFill Interbody Fusion Device |
Pinnacle Spine Group, LLC |
| K133721 |
12/05/2013 |
INFILL 41-TLIF CONVEX OBLIQUE DEVICE, INFILL 43-TLIF CONTOUR OBLIQUE, INFILL 44-TLIF CONTOUR OBLIQUE AND THE INFILL 60 |
PINNACLE SPINE GROUP, LLC |
| K143488 |
12/08/2014 |
InFill Graft Delivery System |
PINNACLE SPINE GROUP, LLC |
| K103729 |
12/22/2010 |
INFILL INTERVERTEBRAL BODY FUSION DEVICE |
PINNACLE SPINE GROUP, LLC |
| K124012 |
12/27/2012 |
INFILL OBLIQUE TLIF DEVICE |
PINNACLE SPINE GROUP, LLC |
| K111632 |
06/13/2011 |
INFILL GRAFT DELIVERY SYSTEM |
PINNACLE SPINE GROUP, LLC |
| K150206 |
01/29/2015 |
InFill Interbody Fusion Devices |
PINNACLE SPINE GROUP, LLC |
| K172349 |
08/03/2017 |
InFill« Interbody Fusion Device |
Pinnacle Spine Group, LLC |
|
|
