Rsb Spine, LLC - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Rsb Spine, LLC has 7 FDA 510(k) cleared medical devices. Based in Chseterland, US.
Historical record: 7 cleared submissions from 2006 to 2010. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Rsb Spine, LLC Filter by specialty or product code using the sidebar.
7 devices
Cleared
Jan 27, 2010
C-PS PEEK OPTIMA CERVICAL INTERBODY SPACER, L-PS PEEK OPTIMA LUMBAR INTERBODY...
Orthopedic
161d
Cleared
Oct 06, 2009
INTERPLATE C
Orthopedic
90d
Cleared
May 29, 2008
INTERPLATE PEEK CERVICAL INTERBODY FUSION DEVICE (IFD)
Orthopedic
31d
Cleared
Sep 18, 2007
INTERPLATE INTERBODY FUSION DEVICE, MODELS C, CGC, L AND LGC
Orthopedic
68d
Cleared
Jun 11, 2007
MODIFICATION TO: INTERPLATE VBR SYSTEM
Orthopedic
26d
Cleared
Apr 19, 2007
INTERPLATE VBR SYSTEM
Orthopedic
77d
Cleared
Aug 18, 2006
INTERPLATE VBR SYSTEM
Orthopedic
91d