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
1919332895
Device Listing 1919332895
Listing Summary
#
Listing key
1919332895
Premarket submission
K162264
Device
Cascadia Interbody System
Applicant
K2m, Inc.
Product code
MAX
Decision date
2016-09-21
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