FDA 510(k) Applications Submitted by RSB SPINE LLC.

FDA 510(k) Number Submission Date Device Name Applicant
K071372 05/16/2007 MODIFICATION TO: INTERPLATE VBR SYSTEM RSB SPINE LLC.
K092540 08/19/2009 C-PS PEEK OPTIMA CERVICAL INTERBODY SPACER, L-PS PEEK OPTIMA LUMBAR INTERBODY SPACER RSB SPINE LLC.
K070316 02/01/2007 INTERPLATE VBR SYSTEM RSB SPINE LLC.
K081194 04/28/2008 INTERPLATE PEEK CERVICAL INTERBODY FUSION DEVICE (IFD) RSB SPINE LLC.
K061401 05/19/2006 INTERPLATE VBR SYSTEM RSB SPINE LLC.
K092070 07/08/2009 INTERPLATE C RSB SPINE LLC.
K071922 07/12/2007 INTERPLATE INTERBODY FUSION DEVICE, MODELS C, CGC, L AND LGC RSB SPINE LLC.


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