Pinnacle Spine Group, LLC - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Pinnacle Spine Group, LLC has 12 FDA 510(k) cleared orthopedic devices. Based in Dallas, US.
Historical record: 12 cleared submissions from 2011 to 2017.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
12 devices
Cleared
Dec 14, 2017
InFill® Interbody Fusion Device
Orthopedic
133d
Cleared
Nov 19, 2015
InFill Interbody Fusion Device
Orthopedic
100d
Cleared
Jul 14, 2015
InFill Interbody Fusion Devices
Orthopedic
71d
Cleared
Apr 03, 2015
InFill Interbody Fusion Devices
Orthopedic
64d
Cleared
Dec 17, 2014
InFill Graft Delivery System
General Hospital
9d
Cleared
May 05, 2014
INFILL CERVICAL
Orthopedic
115d
Cleared
Mar 31, 2014
INFILL 41-TLIF CONVEX OBLIQUE DEVICE, INFILL 43-TLIF CONTOUR OBLIQUE, INFILL...
Orthopedic
116d
Cleared
Jun 04, 2013
INFILL OBLIQUE TLIF DEVICE
Orthopedic
159d
Cleared
Aug 29, 2012
INFILL GRAFT DELIVERY SYSTEM
General Hospital
103d
Cleared
Jul 13, 2012
INFILL INTERVERTEBRAL BODY FUSION DEVICE
Orthopedic
30d
Cleared
Aug 11, 2011
INFILL GRAFT DELIVERY SYSTEM
General Hospital
59d
Cleared
Apr 18, 2011
INFILL INTERVERTEBRAL BODY FUSION DEVICE
Orthopedic
117d