Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
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.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact