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
1468223202
Device Listing 1468223202
Listing Summary
#
Listing key
1468223202
Premarket submission
K172104
Device
Ozark(tm) Cervical Plate System
Applicant
K2m, Inc.
Product code
KWQ
Decision date
2017-08-23
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
3765
9617544
3003112432
Oonagh Lahiff
1
N
2020-04-25
2 Pearl Court Allendale NJ US 07401
225006
3004774118
3008599177
K2M, INC.
1
N
2020-04-25
600 Hope Pkwy SE Leesburg VA US 20175