Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
2035225813
Device Listing 2035225813
Listing Summary
#
Listing key
2035225813
Premarket submission
K152568
Device
C-VBR
Applicant
Cardinal Spine, LLC
Product code
PLR
Decision date
2016-02-11
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
225006
3004774118
3008599177
K2M, INC.
1
N
2020-04-25
600 Hope Pkwy SE Leesburg VA US 20175