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
1049058513
Device Listing 1049058513
Listing Summary
#
Listing key
1049058513
Premarket submission
K171556
Device
K2M Navigation Instruments
Applicant
K2m
Product code
OLO
Decision date
2018-01-16
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